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Human Volunteers

Human Volunteers: Indivuidals who particpate in research studies or clinical trials, often providing valuable insights and data to advance scientific understanding.
These volunteers play a crucial role in medical and social research, contributing their time and effort to help researchers investigate new treatments, therapies, or behaviors.
The participation of human volunteers is essential for ensuring the safety and efficacy of new interventions, as well as understanding the human experience in various contexts.
Researchers rely on the altruism and cooperation of these volunteers to drive progress in fields such as healthcare, psychology, and social sciences.

Most cited protocols related to «Human Volunteers»

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Publication 2010
Adult Aluminum Biological Assay BLOOD Blood Platelet Disorders Blood Platelets Calculi Deceleration Dextran Donors Electricity Ethics Committees, Research Gel Chromatography Hemodynamics Human Volunteers Medical Devices physiology Platelet-Rich Plasma Platelet Activation Sepharose Systole Thromboplastin Torque Viscosity Voluntary Workers
Nineteen sequentially collected blood samples from a human volunteer who was experimentally infected with P. falciparum 3D7 were used for the validation of the quantitative PCR assays. This volunteer was a participant in a larger study of the in vivo efficacy of anti-malarial drug, to be described in more detail elsewhere [McCarthy et al, manuscript in preparation]. Briefly, a blood sample was taken pre-infection and then every 12 hours from Day 3 at 8 am, for 10 consecutive days. Anti-malarial treatment was administered on Day 7 at 8 pm, and two extra blood samples were collected post treatment at +6 and +18 hours). Following extraction of the parasite DNA in these samples, extracts were tested in triplicate to validate the rt-qPCR assays. Thick and thin blood film preparations were also used to monitor the volunteer's parasitaemia at each time point.
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Publication 2011
Antimalarials Biological Assay BLOOD Human Volunteers Infection Parasitemia Parasites Pharmaceutical Preparations Voluntary Workers
We introduced the blend into two experimental huts in which there were single human volunteers sleeping under non-insecticidal bed-nets, such that in each hut, the blend and the human volunteer were positioned four meters apart. Two light traps were set up to collect mosquitoes inside each hut: one of the light traps near the human volunteer, and the other near the blend. In another two experimental huts, we set up a similar arrangement with single human volunteers but without introducing the blend. Instead, a blank unbaited MM-X® was set up at a similar location as in the first two huts, and similarly two light traps were set up in these huts. The volunteers remained in the same huts but the synthetic blend was rotated between the huts every night so as to account for any positional bias on mosquito catches. Again, for each experimental night mosquitoes entering the huts were trapped between 7.00pm and 7.00am. The mosquitoes were sorted into different taxa and counted daily. These experiments were repeated for a total of sixteen nights.
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Publication 2010
Culicidae Human Volunteers Insecticides Light SLC6A2 protein, human Voluntary Workers
The MET is composed of four wooden panel frames measuring 35 × 35 cm, arranged to form a square cavity into which human volunteers’ legs are placed (Fig. 2c). The panels hold sets of vertical parallel stainless steel wires spaced 5 mm apart, which are electrically connected to a 24 V battery-powered stable direct current (DC) power source, thereby creating an electric potential between the wires, which is sufficient enough to kill mosquitoes trying to pass through the wires, but without destroying the specimen, as observed with previous prototypes [68 (link)]. The power is supplied at low output, which is sufficient to kill mosquitoes on contact but poses no harm if accidentally contacted by volunteer. This combination of voltage with current setting was identified through pilot laboratory experiments using insectary-reared An. gambiae and An. arabiensis specimens with an a prior minimum kill probability threshold of 80 % [80 ]. The MET prototype used was modified to improve upon shortcomings reported in an earlier version which included the tendency to short circuit and weak physical stability [68 (link)]. Specific changes were: (1) introduction of hinges to secure the four angles of the main frame (Fig. 2a), and (2) better alignment of grid wires into the frame using grooves which minimized the possibility of opposing wires contacting each other and short circuiting. During mosquito trapping, each MET unit was placed on a 2 m × 2 m wooden frame platform placed on a white sheet (Fig. 2c) which made it easier for collectors to see the electrocuted mosquitoes that dropped on the floor. The four legs of the platform were placed in water bowls to create a barrier that prevented ants from crawling onto it and consuming dead mosquito samples. During mosquito collection, a volunteer sits with their lower limbs placed inside the square trapping box (Fig. 2c) to act as attractive bait. Mosquitoes were captured by a single adult male per location using a MET over a 12-h period on each night of experiments (18:00–06:00 h). Sampling was conducted for 45 min of each hour, followed by a 15-min break period during which the trap was turned off, and mosquitoes collected either from the floor of the platform where they had fallen after electrocution, or from the grid panel surfaces using forceps. This 15-min break also allowed for exchange of collectors between matched indoor and outdoor stations at each house after each hour.

Step-wise setting and improvement made to the mosquito electrocuting trap (MET). a Locking together of hinges connecting individual panels with bolts; b locking of assembled panels into the main, outer frame; c fully assembled MET in use by a human participant wearing protective clothes except for on his feet, which are placed within the MET frame

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Publication 2016
Adult Ants Culicidae Debility Dental Caries Electricity Foot Forceps Homo sapiens Human Volunteers Leg Lower Extremity Males Physical Examination Reading Frames Stainless Steel Voluntary Workers
To measure bacterial replication and survival ex vivo, 0.5 ml of freshly drawn mouse or human blood anticoagulated with 0.005 mg desirudin per ml was incubated with 50 µl of a bacterial suspension containing 5 × 105 CFU (mouse) or 5 × 106 CFU (human). Where indicated, human blood was processed to generate desirudin-plasma or serum. Where indicated, 5% Alexa Fluor 488–conjugated human fibrinogen (Life Technologies), CD (0.04 mM), or purified mouse monoclonal antibodies (∼10 µg ml−1 final concentration) were added to the samples. After incubation at 37°C for 0, 30, or 60 min, 0.5 ml of PBS with 0.5% saponin or 0.5 ml agglutination lysis buffer (0.5% saponin, 200 U SK K, 100 µg trypsin, 2 µg DNase, 10 µg RNase per ml PBS) were added to each sample for 10 min at 37°C before plating on agar for enumeration of CFU. Treatment with agglutination lysis buffer is annotated as +SK in the figures. Statistical analysis was performed by two-tailed Student’s t test. For flow cytometry analysis, samples were incubated first with lysostaphin (10 µg ml−1) for 5 min to lyse extracellular bacteria and next with erythrocyte lysis buffer (QIAGEN) for 30 min on ice. Blood leukocytes were recovered after centrifugation at 400 g, washed three times, and suspended in PBS containing 1% FBS. Cells were stained with allophycocyanin-conjugated α-GR1 and analyzed using a FACSCanto (BD). The data were analyzed with the two-tailed Student’s t test. Human volunteers were enrolled under a protocol that was reviewed and approved by the University of Chicago's Institutional Review Board.
Publication 2016
Agar Agglutination alexa fluor 488 allophycocyanin Bacteria BLOOD Buffers Cells Centrifugation Deoxyribonucleases desirudin DNA Replication Endoribonucleases Erythrocytes Ethics Committees, Research Fibrinogen Flow Cytometry Homo sapiens Human Volunteers Leukocytes Lysostaphin Monoclonal Antibodies Mus Plasma Saponin Serum Student Trypsin

Most recents protocols related to «Human Volunteers»

Example 8

To demonstrate safety and efficiency of the mRNA vaccine composition(s), a clinical trial (phase I) is initiated. In the clinical trial, a cohort of human volunteers is intradermally or intramuscularly injected for at least two times. In order to assess the safety profile of the vaccine compositions according to the invention, subjects are monitored after administration (vital signs, vaccination site tolerability assessments, hematologic analysis). The efficacy of the immunization is analyzed by determination of virus neutralizing titers (VNT) in sera from vaccinated subjects. Blood samples are collected on day 0 as baseline and after completed vaccination. Sera are analyzed for virus neutralizing antibodies.

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Patent 2024
Antibodies, Neutralizing BLOOD Hendra Virus Human Volunteers Immunization mRNA Vaccine Nipah Virus Safety Serum Signs, Vital Vaccination Vaccines Virus

Example 15

To demonstrate safety and efficiency of the mRNA vaccine composition(s), a clinical trial (phase I) is initiated. In the clinical trial, a cohort of human volunteers is intramuscularly injected for at least two times (e.g. day 0 and day 28) with mRNA encoding variant SARS-CoV-2 spike protein formulated in LNPs according to the invention. In order to assess the safety profile of the vaccine compositions according to the invention, subjects are monitored after administration (vital signs, vaccination site tolerability assessments, hematologic analysis). The efficacy of the immunization is analyzed by determination of virus neutralizing titers (VNT) in sera from vaccinated subjects. Blood samples are collected on day 0 as baseline and after completed vaccination. Sera are analyzed for virus neutralizing antibodies.

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Patent 2024
Antibodies, Neutralizing BLOOD Human Volunteers Immunization mRNA Vaccine RNA, Messenger Safety Serum Signs, Vital spike protein, SARS-CoV-2 Vaccination Vaccines Virus
To the best of our knowledge a validated, widely-implemented, objective, tool to evaluate outcome of such procedures in children is yet to be established. However, to enable comparability of our results with those reported previously, we have used a modified version of the assessment tool developed by Percival et al. [13 (link), 14 (link)]. We also evaluated whether MTP transfer impacts on hand dominancy and assessed whether patients showed preference for using the hand that was operated on. The sensibility was examined and recorded in terms of having a two-point discriminatory capacity of < 5 mm.
We certify that all applicable institutional and governmental regulations concerning the ethical use of human volunteers were followed during this research. Informed written consent was obtained from all participants parents and the Ethical Committee of Tehran University of Medical Sciences approved this study. Parents of the children of whom pictures or videos are to be published have given their written consent. The study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki.
The parents/guardians of the children provided informed written consent to participate. We obtained consent for publication from the parents/guardians of the children included in the study to publish the photos of participants.
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Publication 2023
Child Human Volunteers Legal Guardians Parent Patients
This is a report on a small series of cases with hypoplastic thumb (Fig. 1) treated with a metatarsophalangeal transfer. We hereby certify that all applicable institutional and governmental regulations concerning the ethical use of human volunteers were followed during this research. Ethics committee of the Arak University of the medical Science approved the design of the study (IR.ARAKMU.REC.1400.230). Informed written consent was obtained from all participants.

Hypoplastic thumb: an underdeveloped, floating, nonfunctioning thumb with no bony or muscular support, attached to the hand by only skin and soft tissue

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Publication 2023
Bones Ethics Committees Human Volunteers hypoplasia Muscle Tissue Skin Thumb Tissues
A fully balanced cross-over dose–response experiment was conducted using two I-LACT chambers of the SFS, one for the treatment and one for the control, whereby mosquitoes could interact with the human volunteers (Fig. 2). As previous experiments did not show any difference in the numbers of mosquitoes collected between the chambers, the treated and untreated emanators were fixed to the respective chambers for the duration of the experiment to avoid any potential contamination. Each experimental day, one replicate for biting and one for landing was conducted with the same volunteers. A replicate comprised 1 h of exposure to either the treatment (transfluthrin) or the negative control. To simulate an outdoor peridomestic setting, biting or landing was conducted 2 m from the end inside the I-LACT (Fig. 3). Four doses of transfluthrin-treated emanators (5 g, 10 g, 15 g and 20 g) were evaluated consecutively. Each dose was tested for six replicates, after which the emanator with the next highest concentration of transfluthrin was used.

Flow chart showing the various iterations of the experiments conducted in this study

Schematic representation of the I-LACT used for the experiments. a Setup of the experiment with transfluthrin-impregnated eave-positioned targeted insecticide (EPTI) strips against Anopheles mosquitoes. b Setup of the experiment with freestanding transfluthrin passive emanators (FTPE) against Aedes aegypti

Two male volunteers aged 25–40 years were recruited by written informed consent. The volunteers were non-smokers and non-alcohol drinkers, and did not use perfumed cosmetics prior to the experiment to minimize heterogeneity in their attraction to mosquitoes [29 (link)]. To standardize the area available to the mosquitoes for biting (knees and ankles), the volunteers wore closed shoes and a bug jacket (Fig. 3). The volunteers were rotated between compartments (treatments) after each experimental day (one day for landing and the following day for biting) to account for differential attractiveness to mosquitoes between individuals [30 (link)]. Temperature and humidity were recorded inside one of the I-LACT using a Tiny Tag Gemini Data Logger (Chichester, West Sussex, UK). To ensure transfluthrin vaporization, the experiments were conducted at temperatures above 23 ºC [31 (link)].
On each experimental day, the treatment and control were allocated to one of the two chambers of the I-LACT 45 min before the experiment commenced, to allow emanation of the transfluthrin to have started before the experiment began. The experiment started when the volunteer sat down on the chair and the mosquitoes were released into the chamber of the I-LACT from the release cages, which were opened by pulling a string (Fig. 3).
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Publication 2023
Aedes Ankle Anopheles Crossing Over, Genetic Culicidae DNA Replication Ethanol Genetic Heterogeneity Human Volunteers Humidity Insecticides Knee Males Non-Smokers transfluthrin Vaporization Voluntary Workers

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More about "Human Volunteers"

Human volunteers, also known as research participants or clinical trial subjects, play a pivotal role in advancing scientific understanding and medical progress.
These altruistic individuals contribute their time, effort, and personal experiences to help researchers investigate new treatments, therapies, and behaviors.
The participation of human volunteers is essential for ensuring the safety and efficacy of novel interventions, as well as gaining insights into the human experience across various contexts.
Researchers rely on the cooperation and generousity of these volunteers to drive progress in fields such as healthcare, psychology, and social sciences.
The utilization of human volunteers often involves the use of various laboratory techniques and reagents, such as FBS (Fetal Bovine Serum) for cell culture, RPMI 1640 media for maintaining cell lines, IL-2 (Interleukin-2) for T-cell activation, Trypsin-EDTA for cell detachment, Ficoll-Paque Plus for density gradient centrifugation, Penicillin and Streptomycin for antimicrobial protection, Histopaque-1077 for isolating mononuclear cells, and GlutaMAX-I for enhancing cell growth.
Additionally, tools like the MinElute PCR Purification Kit may be employed to purify and concentrate DNA samples obtained from volunteer specimens.
These human volunteers, through their selfless contribution, enable researchers to advance scientific knowledge and develop innovative solutions that can ultimately improve human health and well-being.
Their participation is truly invaluable and deserves recognition and appreciation.