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Rectal Prolapse clinical trials

View clinical trials related to Rectal Prolapse.

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NCT ID: NCT03487640 Completed - Clinical trials for Constipation by Outlet Obstruction

Surgical Treatment for ODS With Rectal Prolapse Surgical Treatment for Rectal Prolapse

Start date: January 8, 2018
Phase:
Study type: Observational

Chronic obstinate constipation is hard to deal with in clinic. Especially for obstructed defecation syndrome(ODS). Rectal prolapse is the most common type of ODS. Lots of surgical procedures have been suggested for it but with unsatisfactory results.To develop new surgical treatment and to provide higher quality proof for this intractable condition is of significance.

NCT ID: NCT03383926 Completed - Hemorrhoids Clinical Trials

Longo's Intervention in the Treatment of Hemorrhoids and Rectal Mucosal Prolapse

Start date: April 4, 2004
Phase: N/A
Study type: Interventional

The aim of this study is to define the significance of the distance of the staple line to the dentate line of the anal canal in the efficacy of the Longo's intervention.

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: 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: 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: 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.

NCT ID: NCT01301417 Completed - Lymphoma Clinical Trials

Data Collection of Patients Treated With the ColonRing™ for the Creation of Circular Compression Anastomosis

RETROPRESS
Start date: February 2011
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 a single center. The data will assist in further evaluating the performance of the ColonRing™ device in regards to the creation of a colorectal anastomosis. 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: NCT01056913 Completed - Clinical trials for Inflammatory Bowel Diseases

NITI CAR27 (ColonRing) Compression Anastomosis in Colorectal Surgery

Start date: October 2008
Phase: Phase 4
Study type: Interventional

After resection of diseased segments of the large intestine, the continuity of the intestine has to be restored. This can be done by suturing or with so called stapling devices. In addition since 2 centuries compression rings are used to connect the intestine after resection. The NITICAR27 device is a novel compression anastomosis device. The investigators want to prove if this novel device can be compared to commonly used stapling devices concerning anastomotic leakage, bleeding and stenosis.