Evaluating long-term outcomes of STARR surgery for rectocele treatment
Single-center Retrospective Study of the Long-term Results of the Stapled TransAnal Rectal Resection (STARR) Operation Proposed in the Treatment of a Rectocele in Consecutive Patients
This study looks at how well the STARR surgery works in the long run for people with rectocele.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 77 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | University Hospital, Grenoble Academic / other |
| Locations | 1 site (Grenoble) |
| Trial ID | NCT05037422 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the long-term technical and functional results of the Stapled Transanal Rectal Resection (STARR) operation in patients with rectocele. The STARR technique involves a transanal approach to rectal resection using a stapler, which is a less invasive option for treating rectal static disorders. The study will analyze data from a series of consecutive cases performed at an expert center to provide insights into the effectiveness of this procedure, addressing the gaps identified by the American Gastroenterology Association regarding the insufficiency of patient services and the predominance of short-term studies.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 18 and over who have undergone STARR surgery for rectocele at least 10 years prior.
Not a fit: Patients who have objections to participating in the study or have not undergone the STARR procedure will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable long-term data that may improve treatment options and quality of life for patients suffering from rectocele.
How similar studies have performed: While there is limited long-term data available, previous studies on similar surgical techniques have shown promising results, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient operated for rectocele for 10 or more * Age 18 and over * Informed patients Exclusion Criteria: * Patient objection
Where this trial is running
Grenoble
- CHU Grenoble Alpes, Service de chirurgie digestive et de l'urgence — Grenoble, France (Recruiting)
Study contacts
- Principal investigator: Jean-Luc Faucheron, MD — CHU Grenoble Alpes
- Study coordinator: Sandrine BARBOIS, MD
- Email: sandrinebarbois@yahoo.fr
- Phone: 0033476765526
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.