Clinical Trials Directory

Trials / Terminated

TerminatedNCT02254928

Corifollitropin Alfa Versus Daily rFSH in the Controlled Ovarian Stimulation of Poor Responders

Comparative Study Between the Use of Corifollitropin Alfa and Daily Recombinant FSH in the Controlled Ovarian Stimulation of Poor Responders

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
26 (actual)
Sponsor
Vida Recoletas Sevilla · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

A randomised, crossover, multicentre, national, clinical trial comparing the efficacy of corifollitropin alfa versus daily recombinant FSH and HMG in the controlled ovarian stimulation of women with a poor ovarian response undergoing IVF treatments. The main objective of this study is comparing the number of oocytes obtained after the follicle puncture when using each of these two stimulation protocols. Only poor responders according to the Bologna criteria will be recruited for this trial. All participants will undergo two stimulation cycles to obtain and accumulate oocytes by vitrification. One of the cycles will be done with the corifollitropin alfa protocol and the other with daily rFSH and HMG, the order of application of these protocols will be randomised (crossover clinical trial) in each patient.

Conditions

Interventions

TypeNameDescription
DRUGCorifollitropin alfaOne dose of 150 μg of corifollitropin alfa will be administered at day 1 of stimulation. Stimulation will be continued with 250-300 IU/day of rFSH from day 8 forward.

Timeline

Start date
2014-09-01
Primary completion
2015-07-01
Completion
2015-11-01
First posted
2014-10-02
Last updated
2016-01-18

Locations

4 sites across 1 country: Spain

Source: ClinicalTrials.gov record NCT02254928. Inclusion in this directory is not an endorsement.