Using a Nanoscope System for Sacrospinofixation
Visualization by the Nanoscope System During Sacrospinofixation
This study is testing a new tiny camera system during surgery for vaginal prolapse to see if it helps doctors fix things more accurately and safely for women.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | Female |
| Sponsor | Hospices Civils de Lyon Academic / other |
| Locations | 1 site (Lyon) |
| Trial ID | NCT06177340 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on the use of a nanoscale visualization system during sacrospinofixation, a surgical technique for treating vaginal prolapse. The aim is to improve the precision of fixing a non-absorbable thread to the sacrosciatic ligament, which is crucial for preventing recurrence of prolapse and minimizing complications. By providing clear visual control, the study seeks to reduce risks associated with the procedure, such as vascular and nerve injuries. Women who have undergone this procedure with the nanoscale system will be evaluated to assess outcomes and complications.
Who should consider this trial
Good fit: Ideal candidates for this study are women over 18 who have previously undergone anterior and/or posterior sacrospinofixation using the nanoscale system.
Not a fit: Patients who may not benefit from this study include those unable to understand the information provided or those under guardianship.
Why it matters
Potential benefit: If successful, this approach could lead to improved surgical outcomes and reduced complications for women undergoing sacrospinofixation.
How similar studies have performed: While this approach is innovative, similar studies have not been widely reported, indicating that this may be a novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * women over 18 * patient who benefited from anterior and/or posterior sacrospinofixation using the nanoscope system * person having expressed his non-opposition Exclusion Criteria: * inability to understand the information given * person deprived of liberty * person under guardianship
Where this trial is running
Lyon
- Hôpital Femme Mère Enfant — Lyon, France (Recruiting)
Study contacts
- Study coordinator: Gautier CHENE, MD, PhD
- Email: gautier.chene@chu-lyon.fr
- Phone: +33 (4) 72 35 58 70
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.