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Search / Trial NCT03998761

Progesterone Versus Progesterone Plus Dydrogesterone in FET

Launched by MỸ ĐỨC HOSPITAL · Jun 24, 2019

Trial Information

Current as of April 25, 2025

Completed

Keywords

Fet Micronized Progesterone Dydrogesterone

ClinConnect Summary

All patients undergoing FET will receive oral estradiol valerate (Valiera®; Laboratories Recalcine) 8 mg/day from the second or third day of menses for 6 days. Endometrial thickness will be monitored from day six onwards. From day 8-9 of menses, the estradiol dose could be adjusted from 8mg/day to 16mg/day according the development of the endometrium. Progesterone will be started when endometrial thickness reached 8 mm or more. In the first four months, all the patients will be treated with micronized progesterone. In five months later, the intervention will be changed to micronized progest...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Undergoing frozen embryo transfer
  • Endometrial prepared by exogenous hormonal regimen
  • Permanent resident in Vietnam
  • Exclusion Criteria:
  • Having \> 2 embryo transfer attempts
  • Having embryo(s) from donors cycles
  • Having embryo(s) from IVM
  • Having embryo(s) from PGT/PGS
  • Having endometrial abnormalities: polyp, sub-mucosal fibroid, cesarean scar defects, endometrial hyperplasia, endometrial fluid accumulation, endometrial adhesion.
  • Participating in another IVF study at the same time

About Mỹ đức Hospital

Mỹ Đức Hospital is a leading healthcare institution dedicated to advancing medical research and improving patient outcomes through innovative clinical trials. With a strong emphasis on ethical practices and patient safety, the hospital collaborates with reputable research organizations and healthcare professionals to conduct studies across various therapeutic areas. Committed to excellence in clinical research, Mỹ Đức Hospital leverages its state-of-the-art facilities and experienced staff to contribute valuable insights that enhance medical knowledge and treatment options for diverse patient populations.

Locations

Ho Chi Minh City, Tan Binh, Vietnam

Patients applied

0 patients applied

Trial Officials

Tuong M Ho, MD

Study Chair

Hope Research Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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