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Fyremadel

Manufactured by Ferring
Sourced in United Kingdom

Fyremadel is a laboratory equipment product designed for specific scientific applications. It serves a core function within the research and testing activities conducted in various laboratories. The details and intended use of Fyremadel are not available in this factual and unbiased response.

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2 protocols using fyremadel

1

Oocyte Donation and Retrieval Protocol

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Immature oocytes at GV or MI stages were donated by healthy non-diabetic women aged 25–39 years after signed informed consent. The women were undergoing controlled ovarian stimulation (COH) treatments aimed at oocyte cryopreservation or intracytoplasmic sperm injection (ICSI) at the Department of Reproductive Medicine of Karolinska University Hospital. The standard COS treatments and clinical routines have been previously described (Feichtinger et al, 2017 (link)). Briefly, either a long-protocol, using a nasal GnRH agonist (Nafarelin 800 μg daily; Synarela, Pfizer) or buserelin 1200 μg daily; Suprecur, Sanofi), or a short protocol using GnRH antagonist (0.25 mg once daily, SC ganirelix, Fyremadel, Ferring) initiated routinely on the fifth day of COS were conducted. The dose of COS (75–400 IU daily of recombinant follicle stimulating hormone (Gonal-F Merck or hMG Menopur, Ferring) was individualized to patient’s age, menstrual cycle length, antral follicle count and anti-Mullerian hormone levels. Ovarian follicle growth tracking was performed by scheduled transvaginal ultrasound examinations that lead to the planning timepoint for oocyte maturation triggered by administration of recombinant hCG (250 μg SC Ovitrelle; Merck). Oocyte retrieval was carried out by transvaginal ultrasographically-guided follicular puncture 37 h later.
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2

Ovarian Stimulation Protocol with GnRH Antagonist

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In all cases an antagonist protocol was used to carry out ovarian stimulation. Individualized doses of gonadotrophins were determined by an experienced specialist physician. Transvaginal ultrasound for cycle monitoring was performed every 2 days starting on stimulation day 5. Fixed daily doses of 0.25 mg of gonadotrophinreleasing hormone (GnRH) antagonist (Orgalutran, Cetrotide, Merck Serono Europe Ltd, London, UK; or Fyremadel, Ferring, Malmö, Sweden) were started when the leading follicle reached a mean diameter of 13-14 mm. All patients received GnRH agonist 0.2 mg (Decapeptyl, Ipsen PharmaParis, France) to achieve final oocyte maturation when the mean size of at least two follicles was 18 mm. Oocyte retrieval was performed 36 h later under ultrasound guidance.
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