Using ultrasound to improve office hysteroscopy for patients with previous failures.
Ultrasound Guidance of Office Hysteroscopy in Patients With History of Failure of Office Hysteroscopy Due to Cervical Stenosis.A Randomized Controlled Study
NA · Cairo University · NCT06637111
This study tests if using ultrasound can help patients who have had trouble with previous hysteroscopy procedures successfully access the uterine cavity.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 58 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Cairo University (other) |
| Locations | 2 sites (Cairo and 1 other locations) |
| Trial ID | NCT06637111 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of ultrasound guidance in facilitating office hysteroscopy for patients who have previously experienced failures due to cervical stenosis. Participants will be divided into two groups: one receiving ultrasound-guided hysteroscopy and the other undergoing conventional hysteroscopy. The goal is to determine if ultrasound can improve access to the uterine cavity and enhance the success rate of the procedure. The study aims to provide a more effective approach for patients facing difficulties with traditional methods.
Who should consider this trial
Good fit: Ideal candidates are patients who have previously failed office hysteroscopy due to cervical stenosis.
Not a fit: Patients with pelvic inflammatory disease, severe vaginal bleeding, pregnancy, or allergies to lidocaine, prilocaine, or diclofenac potassium may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve the success rates of office hysteroscopy for patients with a history of procedural failure.
How similar studies have performed: While this approach is innovative, similar studies have not been widely reported, indicating that this may be a novel intervention.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with history of failure of office hysteroscopy Exclusion Criteria: * Pelvic inflammatory disease * Severe vaginal bleeding * Pregnancy * Allergy to lidocaine, prilocaine or diclofenac potassium
Where this trial is running
Cairo and 1 other locations
- Faculty of medicine, Cairo university — Cairo, Egypt (RECRUITING)
- Obstetrics &Gynecology Department , Faculty of medicine ,Cairo university — Cairo, Egypt (RECRUITING)
Study contacts
- Principal investigator: Usama M Fouda — Cairo University
- Study coordinator: Usama M Fouda, Prof.
- Email: umfrfouda@kasralainy.edu.eg
- Phone: 01095401375
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.
Conditions: Hysteroscopy, Ultrasound, Pain