Trial · NCT06227949
FSH and LH Versus FSH Alone for Ovarian Stimulation in Non-hormone Sensitive Onco-fertility Patients
NCT06227949, Phase 3, Not yet recruiting, Ellen Greenblatt
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. FSH and LH Versus FSH Alone for Ovarian Stimulation in Non-hormone Sensitive Onco-fertility Patients. Trials, record NCT06227949. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06227949
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- FSH and LH Versus FSH Alone for Ovarian Stimulation in Non-hormone Sensitive Onco-fertility Patients
- NCT number
- NCT06227949
- Status
- Not yet recruiting
- Phases
- Phase 3
- Enrollment
- 140 participants, estimated
- Lead sponsor
- Ellen Greenblatt
- Conditions
- Fertility Preservation
- Interventions
- Luveris
- First posted
- 2024-01-29
- Last updated
- 2024-01-29
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Total number of mature (MII) oocytes available for cryopreservation | 12hrs after egg retrieval | |
| Secondary | Total number of oocytes retrieved per cycle | 1hr after egg retrieval | |
| Secondary | Ratio of mature (MII) to immature oocytes | 12 hours after egg retrieval | |
| Secondary | Total number of mature oocytes (MII) retrieved per IVF/ICSI cycle | 12 hours after egg retrieval | |
| Secondary | Ratio of mature (MII) to immature oocytes per IVF/ICSI cycle | 12 hours after egg retrieval | |
| Secondary | Number of two pronuclei (2PN) zygotes | 48 hours after egg retrieval | |
| Secondary | Fertilization rate, which will include two outcomes each defined as follows: | 48 hours after egg retrieval | * Definition 1: number of 2PN zygotes divided by the number of mature oocyte(s) fertilized per IVF/ICSI cycle. * Definition 2: number of 2PN zygotes divided by the number of oocytes incubated with at least 10,000 sperm per IVF cycle. |
| Secondary | Total number of day 3 embryos | 72-80 hours after egg retrieval | |
| Secondary | Total number of good quality day 5 embryos available for cryopreservation determined by a blinded embryologist using the classification system by Gardner and Schoolcraft, 1999. | 120-132 hours after egg retrieval | |
| Secondary | Incidence of moderate to critical OHSS based on the classification criteria by Mathur et al. 2005 | 2 weeks after egg retrieval |
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/NCT06227949
GET https://conductscience.org/api/trials/v1/NCT06227949/registered