Actively Recruiting

Age: 18Years - 35Years
FEMALE
Healthy Volunteers
ID06526520

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

Age: 18Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female with regular menstrual cycles
  • Age between 18 and 35 years
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

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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

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