Trial · NCT01623570
Clinical Outcomes in WHO Type I Anovulatory Women Using r-hFSH+r-hLH in a 2:1 Ratio or hMG-HP
NCT01623570, Not applicable, Completed, Centro Riproduzione e Andrologia
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Clinical Outcomes in WHO Type I Anovulatory Women Using r-hFSH+r-hLH in a 2:1 Ratio or hMG-HP. Trials, record NCT01623570. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01623570
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Clinical Outcomes in WHO Type I Anovulatory Women Using r-hFSH+r-hLH in a 2:1 Ratio or hMG-HP
- NCT number
- NCT01623570
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 40 participants, actual
- Lead sponsor
- Centro Riproduzione e Andrologia
- Conditions
- Hypogonadotropic Hypogonadism
- Interventions
- Pergoveris: 150IU r-hFSH + 75IU r-hLH, Menopur: HMG-HP (150 IU)
- First posted
- 2012-06-20
- Last updated
- 2012-06-20
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | E2 in pmol/L | Day after the protocol hCG requirement is met (at least one follicle of 17mm is monitored by ultrasound) | Evaluate the patients steroidogenesis |
| Primary | Number of Follicles > 17mm | last US day before hCG administration | To evaluate the efficacy of the stimulation and maturity of follicles |
| Primary | P4 in nmol/L | Day after the protocol hCG requirement is met (at least one follicle of 17mm by US) | Progesteron level to evaluate the endometrial receptivity |
| Secondary | Endometrial thickness | Day 5 and Day 10 of stimulation treatment | Evaluation of endometrial development and receptivity |
| Secondary | Total number of Follicles | Last US day before hCG administration | To evaluate the overall efficacy of stimulation treatment, also including follicles \< 17mm |
| Secondary | Clinical Pregnancy rate | days 35-42 post hCG | Evaluate the ratio between primary end points and final stimulation outcome |
| Secondary | Occurence of any adverse events (early or late ovarian hyperstimulation syndrome) | Days 15-20 post hCG |
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 |
|---|---|
| 23095369 | 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/NCT01623570
GET https://conductscience.org/api/trials/v1/NCT01623570/registered