Trial · NCT04528849
Comparison of Ovulation Induction Cycle Outcomes Between Early and Late Dose Increments for Low Dose Gonadotropin Step-up Protocol Among Infertile Women Diagnosed With Polycystic Ovary Syndrome: Prospective Randomised Trial
NCT04528849, Not applicable, Unknown, Saglik Bilimleri Universitesi
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Ovulation Induction Cycle Outcomes Between Early and Late Dose Increments for Low Dose Gonadotropin Step-up Protocol Among Infertile Women Diagnosed With Polycystic Ovary Syndrome: Prospective Randomised Trial. Trials, record NCT04528849. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04528849
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
Comparison of Ovulation Induction Cycle Outcomes Between Early and Late Dose Increments for Low Dose Gonadotropin Step-up Protocol Among Infertile Women Diagnosed With Polycystic Ovary Syndrome: Prospective Randomised Trial
- NCT number
- NCT04528849
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 160 participants, estimated
- Lead sponsor
- Saglik Bilimleri Universitesi
- Conditions
- Polycystic Ovary Syndrome, Infertility, Female
- Interventions
- Gonadotropin dose increment timing
- First posted
- 2020-08-27
- Last updated
- 2020-08-27
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of preovulatory follicles | 35 days | Number of \>14 mm sized follicles at the end of the ovulation induction treatment |
| Secondary | Biochemical pregnancy rate | 2 weeks after ovulation triggering | Serum pregnancy test will be performed 2 weeks after ovulation triggering |
| Secondary | Clinical pregnancy rate | 3 weeks after ovulation triggering | Clinical pregnancy rate which will be evaluated 3 weeks after ovulation triggering |
| Secondary | Cycle length in days | 7-35 days | Total number of ovulation induction days until ovulation triggering |
| Secondary | Cycle cancellation | 35 days | Cycle cancellation due to \>=3 preovulatory follicles (\>14 mm in size) at the end of the ovulation induction treatment |
| Secondary | Multiple pregnancy rate | 3 weeks after ovulation triggering | Multiple pregnancy rate which will be evaluated 3 weeks after ovulation triggering |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT04528849
GET https://conductscience.org/api/trials/v1/NCT04528849/registered