A Single-center Randomized Controlled Trial of Vaginal Progesterone to Improve Clinical Pregnancy Outcomes in Patients With Repeated Implantation Failure

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study is a single-center, randomized, controlled prospective study. Those patients with repeated implantation failure (RIF) who will recieve frozen thawed embryo transfer (FET) are enrolled in the study. To determine the effect of vaginal progesterone on the clinical pregnancy outcomes of RIF patients.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 20
Maximum Age: 40
Healthy Volunteers: f
View:

• Aged between 20 and 40 years old;

• BMI: 18-28 kg/m2;

• Consistent with the diagnosis of repeated implantation failure of unknown reasons, the previous embryo transfer situation meets one of the following:

• Total embryos transferred ≥ 4 high-quality cleavage-stage embryos; ≥ 2 blastocysts; ≥ 2 high quality cleavage-stage embryos +≥ 1 blastocysts;

• At least 1 high-quality embryo remained for embryo transfer;

• Volunteer to participate in the study and sign the informed consent form.

Locations
Other Locations
China
Reproductive Medicine Center, The affiliated Drum Towel Hospital of Nanjing University Medical School
RECRUITING
Nanjing
Contact Information
Primary
Chenyang Huang
dianshui19901562@126.com
+862583107188
Backup
Na Kong
xtalkn@163.com
+862583107188
Time Frame
Start Date: 2023-08-01
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 152
Treatments
Experimental: Vaginal progesterone supplementation
90 mg progesterone vaginal sustained-release gel is added daily to induce endometrial transformation and luteal support
No_intervention: Regular progesterone
No additional vaginal progesterone gel, routine endometrial transformation and luteal support drugs
Related Therapeutic Areas
Sponsors
Leads: Nanjing University

This content was sourced from clinicaltrials.gov