Clinical trial Recruiting at 1 site Observational Ages 18 to 42 Women only

Endometrial Waves and Pregnancy in FET Cycles with Hormone Therapy

Official title: Correlation Between Endometrial Peristalsis And Pregnancy Outcomes In Patients Undergoing Frozen Embryo Transfer With Hormone Replacement Therapy for Endometrial Preparation Protocol

Run by Mỹ Đức Hospital · NCT07675213 · Data updated 2026-11-12

This study tests whether patterns of uterine contractions during hormone-prepared frozen embryo transfer affect pregnancy outcomes.

Quick facts

Study typeObservational
Ages18 Years to 42 Years
SexWomen only
Enrollment442 (estimated)
SponsorMỹ Đức Hospital
Academic / other
Locations1 site (Ho Chi Minh City)
StatusRecruiting
StartedJune 30, 2026
Main results expectedJune 1, 2027
Study endsDecember 1, 2027
Registry record updatedJuly 9, 2026
Trial IDNCT07675213 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women 18–42 years old planning a hormone replacement therapy–prepared FET and meeting embryo transfer criteria.

Probably not a fit

Patients with non-responding endometrium or cycles not meeting ultrasound assessment time points may not see a benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective observational study will measure endometrial peristalsis using transvaginal ultrasound at predefined times during hormone replacement therapy–prepared FET cycles. It aims to see if the frequency or direction of uterine contractions relates to implantation and pregnancy success. Eligible participants are women aged 18–42 undergoing FET with HRT and meeting certain embryo transfer criteria. Data on hormone levels and peristaltic patterns will be analyzed to identify possible associations with outcomes. The goal is to clarify whether endometrial activity should be considered in ART planning.

Why it matters

Potential benefit: If associations are found, clinicians may tailor endometrial assessment or timing to improve pregnancy chances in FET cycles.

How similar studies have gone: Prior research suggests endometrial contractions influence implantation in natural cycles; evidence in HRT-prepared FET is limited and this study explores that gap.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Women aged 18 - 42 years old
* Scheduled for frozen embryo transfer cycles using hormone replacement therapy protocol
* Transferred no more than two cleavage embryos or one good-quality blastocyst or no more than two poor-quality blastocysts
* Provision of written informed consent to participate

Exclusion Criteria:

* Having an allergy and contraindications for exogenous hormone administration (e.g., breast cancer, thromboembolic disease)
* Cycles with preimplantation genetic testing, oocyte donation, or in vitro maturation
* Having untreated uterine or adnexal abnormalities (e.g., intrauterine adhesions, unicornuate/ bicornuate/ arcuate uterus, endometrial polyp, large leiomyoma ≥5 cm in diameter, hydrosalpinx, endometrial hyperplasia)
* Use of uterine relaxants or intralipid infusion during the embryo transfer process
* Use of a GnRH-agonist for downregulation within one month

Where it's running

  • IVFMD - My Duc Hospital
    Ho Chi Minh City, Vietnam
    Recruiting

Study contacts

  • Principal investigator: Lan N Vuong, MD, PhD — University of Medicine and Pharmacy at Ho Chi Minh City
  • Study coordinator: Nhi NL Ho, MD
  • Email: drnhiho@gmail.com
  • Phone: +84903497611

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.