Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
ID06373822

New Perspectives in Adenomyosis Pathogenesis With Epigenetic Analysis and miRNAs

Led by Université Catholique de Louvain · Updated on 2024-04-22

50

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to identify differences in circulating microRNAs (miRNAs) in the blood of women with adenomyosis to develop new, noninvasive diagnostic methods. Building on previous findings that miRNAs are abnormally expressed in conditions like endometriosis, this study will compare miRNA expression between patients with adenomyosis and healthy subjects to find potential diagnostic biomarkers. Blood samples will be collected from 50 pre-menopausal women undergoing gynecological surgery, including 25 diagnosed with adenomyosis and 25 without endometrial-related diseases. A single 10 ml blood sample will be taken on the day of surgery, processed to isolate miRNAs using specialized kits, and analyzed using commercial arrays and RT-qPCR to measure expression of around 1000 miRNAs. The study will also investigate the biological functions affected by differentially expressed miRNAs. Participants will have their blood drawn during surgery for sample analysis. Researchers will examine miRNA levels as diagnostic biomarkers throughout the study, which lasts approximately 6.5 years. Samples will be stored carefully, and data will be analyzed to identify miRNAs distinguishing adenomyosis patients from healthy individuals. The findings could support the development of new diagnostic tools or treatments for adenomyosis.

CONDITIONS

Brief Title

New Perspectives in Adenomyosis Pathogenesis With Epigenetic Analysis and miRNAs

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age  18 years
  • Female and pre-menopausal
Not Eligible

You will not qualify if you...

  • Tested positive for HIV or Hepatitis
  • Participated in another clinical study in the past 12 months
  • Have symptoms of endometriosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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)

Diagnostic Evaluation

Duration - 1 day

Participants provide a single blood sample on the day of their scheduled surgical intervention for analysis of circulating miRNAs as potential diagnostic biomarkers.

1 visit (in-person)

Long-term Monitoring

Duration - Approximately 6.5 years

Participants' circulating miRNA levels are analyzed over the course of the study to identify diagnostic biomarkers of adenomyosis.

No additional visits required

Trial Site Locations

Total: 1 location

1

CUSL

Brussels, Woluwe-Saint-Lambert, Belgium, 1200

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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