Understanding pain and outcomes in women with obstructive Müllerian anomalies
Clinical Presentations and Surgical Outcome of Obstructive Müllerian Anomalies: A Prospective Cohort Study
This study looks at how pain levels change before and after surgery in women with obstructive Müllerian anomalies to help doctors better understand and treat this condition.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 36 (estimated) |
| Sex | Female |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Assiut) |
| Trial ID | NCT06110052 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on women diagnosed with obstructive Müllerian anomalies (OMAs) and aims to compare their preoperative and postoperative pain levels using a visual analog scale. It will describe the clinical presentations and prevalence of different subtypes of OMAs, as well as the corrective surgical procedures performed and their short-term outcomes. The study seeks to enhance awareness among healthcare providers regarding the clinical presentations of OMAs to prevent delayed diagnoses and associated complications.
Who should consider this trial
Good fit: Ideal candidates for this study are women diagnosed with obstructive Müllerian anomalies or hemi-obstructive Müllerian anomalies.
Not a fit: Patients who have previously undergone surgical repair for their obstructive Müllerian anomalies will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved diagnosis and treatment options for women suffering from obstructive Müllerian anomalies, ultimately enhancing their quality of life.
How similar studies have performed: While there is limited published data on this specific approach, the study aims to fill a gap in understanding the clinical presentations and outcomes of OMAs, suggesting a novel exploration in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All cases with OMAs or H-OMAs Exclusion Criteria: * Cases who refuse to participate in the study. 2.Cases who underwent previous surgical repair for their OMA or H-OMA.
Where this trial is running
Assiut
- Assiut Medical School — Assiut, Egypt (Recruiting)
Study contacts
- Study coordinator: Dina A Mahmoud, MBBCH
- Email: dinaelsaman@yahoo.com
- Phone: 01090054328
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.