Trial · NCT03555942
Luteal Phase-start Ovarian Stimulation With Corifollitropin Alfa
NCT03555942, Not applicable, Completed, Fundacion Dexeus
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Luteal Phase-start Ovarian Stimulation With Corifollitropin Alfa. Trials, record NCT03555942. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03555942
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Luteal Phase-start Ovarian Stimulation With Corifollitropin Alfa
- NCT number
- NCT03555942
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 44 participants, actual
- Lead sponsor
- Fundacion Dexeus
- Conditions
- Infertility
- Interventions
- Follicular phase corifollitropin alfa, Luteal phase corifollitropin alfa
- First posted
- 2018-06-14
- Last updated
- 2022-03-31
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mean number of euploid embryos | 15-45 days following oocyte retrieval procedure | Number of euploid embryos between oocytes received from follicular phase or luteal phase initiation of ovarian stimulation. |
| Secondary | Number of oocytes | 9 -20 days from initiation of ovarian stimulation | The outcome will be evaluated on the day of oocyte retrieval |
| Secondary | Number of MIIs | 9 -20 days from initiation of ovarian stimulation | The outcome will be evaluated on the day of oocyte retrieval |
| Secondary | Total additional dose of rFSH (IU) | 9 -20 days from initiation of ovarian stimulation | Addition total units of FSH following corifollitropin alfa.The outcome will be evaluated on the day of final oocyte maturation |
| Secondary | Duration of ovarian stimulation | 9 -20 days from initiation of ovarian stimulation | Total days of ovarian stimulation .The outcome will be evaluated on the day of final oocyte maturation |
| Secondary | Endocrine profile at specific intervals | Stimulation day 1, day 6, day 8, and Day of final oocyte maturation (actual day may vary between 9-15) | Estradiol, LH, FSH, Progesterone |
| Secondary | Clinical pregnancy rates following transfer of embryos generated from oocytes from follicular phase vs. luteal phase stimulation | 5-8 weeks after embryo transfer procedure | Clinical pregnancy rates , presence of intrauterine gestational sac with an embryonic pole demonstrating cardiac activity |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 36269092 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03555942
GET https://conductscience.org/api/trials/v1/NCT03555942/registered