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Rectal Prolapse clinical trials

View clinical trials related to Rectal Prolapse.

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NCT ID: NCT02971332 Completed - Rectal Prolapse Clinical Trials

Long Term Results of STARR With Contour Transtar

LTSTARR
Start date: June 2007
Phase: N/A
Study type: Observational

Obstructed defecation syndrome (ODS) is a widespread and disabling syndrome. With this study the investigators want to evaluate the long term results of Stapled Transanal Rectal Resection (STARR) performed with Contour Transtar device in the treatment of ODS. A re-evaluation of 113 patients subjected to STARR from June 2007 to January 2010 was conducted.

NCT ID: NCT02901210 Completed - Rectal Prolapse Clinical Trials

A Modified Technique to Facilitate Pealing of the Rectal Mucosa in Delorme Operation

Start date: January 2015
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the investigator new modification for delorme procedure in patients with rectal prolapse , assessing intra-operative morbidity and recurrence rate .

NCT ID: NCT02870192 Not yet recruiting - Rectal Prolapse Clinical Trials

Intra-operative Adverse Events During Laparoscopic Ventral Mesh Rectopexy

Start date: January 2017
Phase: N/A
Study type: Interventional

Outcomes of laparoscopic ventral mesh rectopexy are well known, but data on intra-operative adverse events is scant. A multicenter pool-analysis of prospectively collected database on 1384 patients with internal/external rectal prolapse toke place. Overall 72 (5%) patients experienced complications, 41 discovered and managed intraoperatively, 22 postoperative complications, and 9 required readmission. Despite accepted lower rate of morbidity, these results come from four well equipped European centers by four surgeons practiced at least 200 LVMR.

NCT ID: NCT02609555 Completed - Rectal Prolapse Clinical Trials

TEM Assisted Perineal Rectopexy in Treatment of Rectal Prolapse

Start date: October 2014
Phase: N/A
Study type: Interventional

Curvilinear incision in the postanal space, through the intersphincteric plane, insertion of Proctoscope of TEM technique and dissection till sacral promontory, insertion of mesh between the rectum and sacrum, post anal repair then anal cerclage width absorbable suture.

NCT ID: NCT02601326 Completed - Clinical trials for Complete Rectal Prolapse

Laparoscopic Ventral Mesh Rectopexy Versus Delorme's Operation in Management of Complete Rectal Prolapse

Start date: January 2012
Phase: N/A
Study type: Interventional

A comparative randomized study between laparoscopic ventral mesh Rectopexy and Delorme's procedure in treatment of complete rectal prolapse to ass both efficacy and complications

NCT ID: NCT01992406 Recruiting - Colon Adenoma Clinical Trials

Feasibility, Safety and Outcome of Transrectal Hybrid-NOTES Anterior Resection

Start date: November 2013
Phase: N/A
Study type: Observational [Patient Registry]

Natural orifice transluminal endoscopic surgery has become an important topic. NOTES access routes give the opportunity to reduce surgical access trauma leading to a more painless surgery and enhancing a fast postoperative recovery. Experience with transvaginal laparoscopic cholecystectomy and transvaginal anterior resection for diverticulitis show that such NOTES procedures are feasible and safe. The complication rate to conventional laparoscopic procedures is similar. Since transvaginal access is impossible in men, an alternative route is missing. There are experimental studies and small case series reporting the feasibility of transrectal anterior resection. However any prospective feasibility study demonstrating the safety of the procedure and functional outcomes (sphincter function) are missing. This study investigates the feasibility, practicability, safety and subjective as well as functional outcome of transrectal hybrid-NOTES anterior resection.

NCT ID: NCT01980043 Completed - Rectal Prolapse Clinical Trials

Endoluminal and Needlescopic Assisted Repair of Rectal Prolapse

Start date: May 20, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and feasibility of endoluminal rectal prolapse repair under sedation and local anesthesia using CO2 colonoscopy to fix the rectum with sutures to the abdominal wall under needlescopic control. Further, investigators will evaluate the short and long-term clinical outcomes after this novel approach to treating rectal prolapse.

NCT ID: NCT01899209 Recruiting - Rectal Prolapse Clinical Trials

Surgical Treatment of Obstructed Defecation Syndrome

PRO-REST
Start date: August 2013
Phase: N/A
Study type: Interventional

Obstructed Defecation is a profoundly disabling condition. Many different surgical procedures has been introduced to treat patients affected by this disease. The most used are STARR and ventral rectopexy. Because of the heterogenity of studies and overall the lack of comparison trials, there is no accepted standard surgical treatment.PRO-REST aimed to compare these two procedures (STARR and Ventral Rectopexy) evaluating functional and anatomical results.

NCT ID: NCT01880918 Recruiting - Lymphoma Clinical Trials

A RETROspective Data Collection of comPRESSion Anastomosis Using the ColonRing

Start date: October 2012
Phase: N/A
Study type: Observational

The proposed study is a post marketing, observational, retrospective data collection intended to gather and record data on patients treated with the ColonRing device in routine clinical practice at 4-6 centers. The data will assist in future evaluating the performance of the ColonRing device in regards to the creation of a colorectal anastomosis in Low Anterior Resection procedures. Hypothesis: The performance of the ColonRing, determined by the rate of complications, will be within the acceptable range reported in the literature for alternative treatment modalities.

NCT ID: NCT01656369 Completed - Rectal Prolapse Clinical Trials

Comparative Study Between Delorme Operation With or Without Postanal Repair in Treatment of Complete Rectal Prolapse

Start date: January 2007
Phase: N/A
Study type: Interventional

The aim of the study is to compare Delorme operation alone or with post anal repair and levatorplasty for treating complete rectal prolapse.consecutive patients who were treated for complete rectal prolapse at the Colorectal Surgery Unit were eligible for the study.The patients were randomized into two groups: Group I: consisted of patients were subjected to delorme operation only. Group II: consisted of patients were subjected to delorme operation with post anal repair and levatorplasty.