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Completed

NCT Number: NCT01816321

Corifollitropin Alfa Followed by Menotropin for Poor Ovarian Responders Trial

In combination with the existing literature, previous work indicates that 1) women with poor ovarian response fulfilling the "Bologna criteria" have very low pregnancy rates, irrespective of age 2) current treatment protocols demonstrate ongoing pregnancy rates that do not exceed 8.5% and 3) corifollitropin alfa followed by hpHMG might increase ongoing pregnancy rates in young patients (<40years old) fulfilling the criteria. These findings provide a strong rationale for a definitive large RCT. The COMPORT study will provide conclusive evidence regarding the superiority or not of this novel protocol with corifollitropin alfa followed by hpHMG for the treatment of young poor ovarian responders fulfilling the Bologna criteria.

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Key information

Age range

18 year–39 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Universitair Ziekenhuis Brussel, Brussels, Belgium

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About this study

Recently, the European Society of Human Reproduction and Embryology developed a new definition in order to select patients suitable for inclusion in future clinical trials as poor ovarian responders, the so-called "Bologna criteria". However, a limited number of studies has been published to date including patients with poor ovarian response according to the "Bologna criteria", whereas no randomized trial is published or ongoing for this population.

Preliminary reports in "Bologna poor responders" highlight the limited prospects for these women. Natural cycle IVF has been shown to result in disappointingly low live birth rates, regardless of patients' age and ovarian stimulation with widely accepted treatment modalities, e.g. short agonist protocol, did not appear demonstrate substantial benefits.

Nonetheless, despite the disappointing results from the vast majority of the preliminary studies in this population, a recent pilot study by our group has shown that a specific protocol may indeed be a promising option for women of younger age fulfilling the "Bologna criteria". Corifollitropin alfa followed by highly purified hMG in an antagonist protocol demonstrated an ongoing pregnancy rate of 28% in women <40years, strongly suggesting the conduction of a future randomized trial testing this novel treatment protocol

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age less than 40 years
  • Fulfillment of the "Bologna criteria" for poor ovarian response.

Based on inclusion criteria two patients' categories are eligible:

  • Women < 40 years old AND ≤3 oocytes in one of the previous cycles AND (Antral follicle count <7 or antimullerian hormone serum values <1.1 ng/ml)
  • Women <40 years old and ≤3 oocytes in two the previous cycles with maximum ovarian stimulation

In addition women less than 40 years old will be considered eligible if they had undergone previous ovarian surgery or chemotherapy (risk factors for poor ovarian response) and have an AMH<1.1ng/ml or an AFC<7, as suggested by the Bologna criteria

Exclusion criteria

  • Uterine abnormalities
  • Recent history of any current untreated endocrine abnormality
  • Unilateral or bilateral hydrosalpinx (visible on transvaginal ultrasound, unless clipped)
  • Contraindications for the use of gonadotropins
  • Recent history of severe disease requiring regular treatment

Treatment and study plan

Corifollitropin alfa

Drug

Corifollitropin alfa 150μg on day 2 of the menstrual cycle (stimulation day 1)

recombinant FSH

Drug

recombinant FSH 300IU/daily from day 2 of the cycle (stimulation day 8)until day of ovulation triggering

Ganirelix

Drug

Ganirelix 0.25mg/daily from day 7 of the cycle(stimulation day 6) until day of ovulation triggering

hp HMG

Drug

hp HMG 300IU/daily from day 9 of the cycle (stimulation day 8)until day of ovulation triggering

Primary outcomes

  1. Ongoing pregnancy

    Time frame: 9-10 weeks of gestation

    The presence of intrauterine gestational sac with an embryonic pole demonstrating cardiac activity at 9-10 weeks of gestation.

Secondary outcomes

  1. Clinical pregnancy

    Time frame: 7 weeks of gestation

    The presence of intrauterine gestational sac at 7 weeks of gestation

  2. Biochemical pregnancy

    Time frame: 2 weeks after embryo transfer

    Positive pregnancy test 2 weeks after embryo transfer

  3. Number of oocytes retrieved

    Time frame: 9 -20 days from initiation of ovarian stimulation

    The outcome will be evaluated on the day of oocyte retrieval

Other outcomes

  1. Cycle cancellation due to poor ovarian response

    Time frame: Day 8-10 of ovarian stimulation

    Number of cycles cancelled due to monofollicular or no follicular development

  2. Number of cycles reaching the stage of embryo transfer

    Time frame: 9 -20 days from initiation of ovarian stimulation

    The outcome will be evaluated 3 days after oocyte retrieval

  3. Number and quality of embryos

    Time frame: Day of embryo transfer

    3 days after oocyte retrieval

  4. Number of cycles with frozen supernumerary embryos

    Time frame: 9 -20 days from initiation of ovarian stimulation

    The outcome will be evaluated 5 days after oocyte retrieval or 2-3 days after embryo transfer in case of an embryo transfer

  5. Endocrine parameters (LH,FSH, E2, Progesterone) during ovarian stimulation

    Time frame: Days 1,6,8,10 of stimulation and day of ovulation triggering

  6. Cycle cancellation due to serious adverse effects of medication

    Time frame: 20-25 days after initiation of stimulation

    20-25 days after the initiation of ovarian stimulation all patients (cycles) will be monitored for the occurence of any adverse effect and cycle cancellation(during ovarian stimulation) due to a serious adverse effect from medication

Sponsors and collaborators

Lead sponsor

Universitair Ziekenhuis Brussel

Other

Collaborators

  • University of Medicine and Pharmacy at Ho Chi Minh City

Registry information

Official study title

Corifollitropin Alfa Followed by Hp-HMG Versus Recombinant FSH in Young Poor Ovarian Responders. A Multicentre Randomized Controlled Clinical Trial

Acronym: COMPORT

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Mar 22, 2013
Registry last updated
Jun 23, 2016

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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