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Senescent Endometrial Cells in Patients with Thin Endometrial Lining

Recruiting
Conditions
Cell Senescence
Asherman's Syndrome
Thin Endometrial Lining
Interventions
Procedure: Endometrial Biopsy
Registration Number
NCT06450301
Lead Sponsor
Trio Fertility
Brief Summary

The goal of this observational study is to determine if thin endometrial lining that is unresponsive to estrogen might be associated with the presence of senescent cells in patients following long-term use of oral contraceptives. The main question it aims to answer is:

Are there any senescent cells present in thin endometrial lining?

During the luteal phase of the cycle, participants will will undergo:

* Gynecologic US to measure the endometrial lining thickness and pattern.

* Endometrial biopsy with Pipelle catheter

Detailed Description

The investigators hypothesized that senescent cells in the endometrium may be the cause of the failure of thin endometrium to respond to normal growth stimuli such as estrogen.

The outcome that research team anticipate to measure is the percentage of senescent cells in the endometrial biopsies of women with thin endometrium compared to the control group biopsies.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
100
Inclusion Criteria
  • Age 18-39
  • BMI - up to 35
  • Thin endometrium after OCP use
  • Asherman's syndrome
  • Women already undergoing endometrial biopsy for infertility testing (eg. EMMA testing)
  • Women with archived endometrial biopsy samples
Exclusion Criteria
  • Women with systemic disease (Rheumatic disease, DM)
  • Women with coagulopathies
  • Women with active pelvic inflammatory process
  • Uterine anomalies
  • Pregnant women
  • Any hormonal contraception use or IUD

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Thin endometrial liningEndometrial BiopsyPatients following long-term use of oral contraceptives with known thin endometrial lining (less than 7mm, confirmed in at least two cycles and unresponsive to estrogen-induced growth). We will ask each woman to undergo an endometrial biopsy as part of the study during their luteal phase.
ControlEndometrial BiopsyPatients already scheduled to undergo an endometrial biopsy for infertility management. We will ask each woman to undergo an endometrial biopsy as part of the study during their luteal phase. In some cases, we may be able to access archived endometrial samples from women in the control group who agree to participate and who have already had an endometrial biopsy.
Asherman's syndromeEndometrial BiopsyPatients with Asherman's syndrome following Dilation and curettage (D\&C). We will ask each woman to undergo an endometrial biopsy as part of the study during their luteal phase.
Primary Outcome Measures
NameTimeMethod
Senescent cells presenceThrough study completion, an average of 3 years.

Percentage of senescent cells in the endometrial biopsies of women with thin endometrium compared to the control group biopsies.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Trio Fertility

🇨🇦

Toronto, Ontario, Canada

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