Corifollitropin alfa
DrugCorifollitropin alfa 150μg on day 2 of the menstrual cycle (stimulation day 1)
NCT Number: NCT01816321
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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Notify Me18 year–39 year
Female
Interventional
Phase 3
Universitair Ziekenhuis Brussel, Brussels, Belgium
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
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Based on inclusion criteria two patients' categories are eligible:
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
Corifollitropin alfa 150μg on day 2 of the menstrual cycle (stimulation day 1)
recombinant FSH 300IU/daily from day 2 of the cycle (stimulation day 8)until day of ovulation triggering
Ganirelix 0.25mg/daily from day 7 of the cycle(stimulation day 6) until day of ovulation triggering
hp HMG 300IU/daily from day 9 of the cycle (stimulation day 8)until day of ovulation triggering
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.
Time frame: 7 weeks of gestation
The presence of intrauterine gestational sac at 7 weeks of gestation
Time frame: 2 weeks after embryo transfer
Positive pregnancy test 2 weeks after embryo transfer
Time frame: 9 -20 days from initiation of ovarian stimulation
The outcome will be evaluated on the day of oocyte retrieval
Time frame: Day 8-10 of ovarian stimulation
Number of cycles cancelled due to monofollicular or no follicular development
Time frame: 9 -20 days from initiation of ovarian stimulation
The outcome will be evaluated 3 days after oocyte retrieval
Time frame: Day of embryo transfer
3 days after oocyte retrieval
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
Time frame: Days 1,6,8,10 of stimulation and day of ovulation triggering
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
Universitair Ziekenhuis Brussel
Other
Corifollitropin Alfa Followed by Hp-HMG Versus Recombinant FSH in Young Poor Ovarian Responders. A Multicentre Randomized Controlled Clinical Trial
Acronym: COMPORT
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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