Trial · NCT07065539
GnRH Agonist Pretreatment Duration and Letrozole Supplementation in Frozen Embryo Transfer for Adenomyosis Patients
NCT07065539, Not applicable, Not yet recruiting, First Affiliated Hospital, Sun Yat-Sen University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. GnRH Agonist Pretreatment Duration and Letrozole Supplementation in Frozen Embryo Transfer for Adenomyosis Patients. Trials, record NCT07065539. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07065539
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- GnRH Agonist Pretreatment Duration and Letrozole Supplementation in Frozen Embryo Transfer for Adenomyosis Patients
- NCT number
- NCT07065539
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 432 participants, estimated
- Lead sponsor
- First Affiliated Hospital, Sun Yat-Sen University
- Conditions
- Adenomyosis of Uterus, Frozen Embryo Transfer (FET)
- Interventions
- GnRH-a-1M, GnRH-a-2M, GnRH-a+LE-1M, GnRH-a+LE-2M
- First posted
- 2025-07-15
- Last updated
- 2025-07-15
Source ClinicalTrials.gov
Registered outcomes21
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Live birth rate | 40 weeks after embryo transfer | |
| Secondary | Cycle Cancellation Rate | 3 weeks after initiating artificial cycle | |
| Secondary | Hypoestrogenic Adverse Event Rate | 4 weeks after 3.75mg GnRH-a intramuscular injection | |
| Secondary | Positive Pregnancy Test Rate | 2 weeks post embryo transfer | |
| Secondary | Embryo Implantation Rate | 3 weeks post embryo transfer | |
| Secondary | Clinical Pregnancy Rate | 5 weeks post embryo transfer | |
| Secondary | Ectopic Pregnancy Rate | 7 weeks' gestation | |
| Secondary | Ongoing Pregnancy Rate | 10 weeks post embryo transfer | |
| Secondary | Miscarriage Rate | Prior to 28 weeks' gestation | |
| Secondary | Drug-Related Venous Thromboembolism (VTE) Rate | Treatment initiation until 10 weeks' gestation |
1 to 10 of 21Source ClinicalTrials.gov
See all 21 registered outcomesOutcomes0
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.
Papers6
The papers the trial lists on ClinicalTrials.gov.
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/NCT07065539
GET https://conductscience.org/api/trials/v1/NCT07065539/registered?page=2