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OpenTrials
Completed

NCT Number: NCT01310647

Antral Follicle Priming Prior to ICSI (Intracytoplasmic Sperm Injection) in Previously Diagnosed Low Responders

The aim of this study is to compare the effectiveness of testosterone,estradiol and a combined treatment with estrogens/progestagens prior to IVF-ICSI in previously diagnosed low responder patients.

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Key information

Age range

18 year–41 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

La Fe University Hospital. Department of Obstetrics and Gynecology

Valencia, 46026, Spain

About this study

During controlled ovarian hyperstimulation (COH), most of the early antral follicles are required to grow coordinately. Marked follicular size discrepancies during COH imply that an important number of follicles undergo unsatisfactory maturation. It has been proved that follicular priming with estradiol during the luteal phase of the cycle prior to COH or testosterone treatment during the early follicular phase of the COH cycle may increase the amount of oocytes and embryos retrieved. Nevertheless there are no prospective studies comparing such approaches. The present study consist of two phases:

The present study consists of two different phases:

  • Phase I: (Non randomized) Identification of confirmed low responder patients. Potential low responder patients will be subjected to an standardized ovarian hyperstimulation protocol
  • Phase II: (Randomized) those patients, once confirmed as low responders, will be offered the opportunity to enter the interventional part of the study, being randomized to three different treatment groups: estradiol, testosterone or combined progestagens and estrogens prior to the IVF-ICSI cycle. The previous cycle (phase I) will be used as a self-control for each patient.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Phase 1 (Non randomized. The patient must fit the first plus at least other 2 criteria)
  • Infertility requiring an IVF/ICSI treatment
  • Age ≥ 38 years
  • Basal FSH ≥ 10 mUI/ml (day 3 of the cycle)
  • Serum AMH ≤ 5 pmol/l
  • Antral follicular count ≤ 6 (day 3 of the cycle)
  • Phase 2 (Randomized. The patient must fit at least one criterion regarding the day of GNRH analogue administration during the cycle performed in Phase 1)
  • Less than 4 follicles which mean diameter measuring more than 16mm
  • Serum estradiol levels ≤ 500 pg/ml
  • 4 MII or less than 4 MII oocytes retrieved

Exclusion criteria

  • Patients suffering of endometriosis
  • Patients having progesterone levels ≤ 4 ng/ml (day 21 of the cycle)
  • Patients having a partner affected by severe oligo/astheno/teratozoospermia

Treatment and study plan

Testosterone

Drug

Transdermal testosterone (20µg/kg/day)from day 24 of the previous cycle to day 2 of the ICSI cycle

Other names: Testopatch, Pierre Fabre Ibérica S.A.

Estradiol

Drug

Transdermal estradiol (200µg/day)from day 20 of the previous cycle to day 3 of the ICSI cycle

Other names: Alcis 100, Chiesi España

CombEq

Drug

(150µg Desogestrel + 30µg Ethinylestradiol)/day during the luteal phase of the two cycles prior to the ICSI.

Valerate estradiol 4mg/day during 10 days, starting the second day of the cycle prios to the ICSI cycle.

Other names: Microdiol, MERCK SHARP & DOHME, Meriestra 2mg, Novartis Farmacéutica, S.A.

Primary outcomes

  1. Number of MII oocytes retrieved

    Time frame: 36h after GnRH analogue administration

Secondary outcomes

  1. Total number of follicles punctured

    Time frame: 36h after GnRH analogue administration

  2. Total number of oocytes retrieved

    Time frame: 36h after GnRH analogue administration

  3. Total number of viable embryos

    Time frame: 48h after follicular puncture

  4. Serum and Follicular hormonal levels (testosterone, androstenedione, estradiol)

    Time frame: 36h after GnRH analogue administration

  5. Granulosa cells genetic expression profile

    Time frame: 36h after GnRH analogue administration

  6. Implantation rate

    Time frame: 15 days after embryo transfer

  7. Pregnancy rate

    Time frame: 15 days after embryo transfer

  8. Clinical pregnancy rate

    Time frame: 5 weeks after embryo transfer

Sponsors and collaborators

Lead sponsor

Instituto de Investigacion Sanitaria La Fe

Other

Registry information

Official study title

Prospective Randomized Controlled Trial of Antral Follicle Priming Prior to IVF-ICSI in Previously Diagnosed Low Responders.

Acronym: FOLLPRIM

Important dates

Study start
2011
Primary completion
2012
Study completion
2014
First posted
Mar 8, 2011
Registry last updated
Feb 28, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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