Actively Recruiting
Relaxin Measurement in Different Endometrial Preparation Approaches for Frozen Embryo Transfer
Led by ART Fertility Clinics LLC · Updated on 2026-05-11
5
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the levels of Relaxin hormone in different methods of preparing the endometrium for frozen embryo transfer (FET) cycles. The study explores whether ovulation with a functional corpus luteum (CL) occurs during a natural proliferative phase (NPP) endometrial preparation, as this remains unclear. The trial also addresses concerns about how preparation methods impact pregnancy outcomes, such as risks for bleeding, miscarriage, and pregnancy-related hypertension. The study observes three types of endometrial preparation: a natural cycle, a natural proliferative phase cycle where follicle growth is monitored and progesterone is given before spontaneous ovulation, and a hormonal replacement therapy (HRT) cycle involving estrogen and progesterone. The NPP protocol includes progesterone alone to induce secretory changes, while the HRT protocol combines estrogen and progesterone. Researchers aim to measure Relaxin levels in these different approaches. Participants will be monitored over 4 to 6 months to measure Relaxin hormone levels. This observational study involves tracking menstrual cycles, hormone exposure, and endometrial changes without altering participants' usual care. The main outcome is Relaxin measurement, which may help understand the presence and role of a functional CL in the different preparation methods. Participant involvement includes hormone exposure monitoring and cycle tracking during the study period.
CONDITIONS
Brief Title
Relaxin Measurement in Different Endometrial Preparation Approaches for Frozen Embryo Transfer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female with regular menstrual cycles
- Age between 18 and 35 years
You will not qualify if you...
- Abnormal findings of the ovaries such as endometriosis
- Intake of any hormones within 3 months before study start
- Desire to become pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 to 6 months
Participants are monitored through different endometrial preparation approaches including natural cycle, natural proliferative phase cycle, or hormonal replacement cycle.
Regular monitoring visits depending on cycle type
Trial Site Locations
Total: 1 location
1
ART Fertiltiy Clinic
Abu Dhabi, Abu Dhabi Emirate, United Arab Emirates, 60202
Actively Recruiting
Research Team
B
Barbara Lawrenz, M.D. PhD
J
Jonalyn Edades, MBA
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here