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Swedish Rectal Prolapse Trial

Primary Purpose

Rectal Prolapse

Status
Terminated
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Suture rectopexy
resection rectopexy
Delorme's operation
Altemeier's operation
Sponsored by
Danderyd Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Prolapse focused on measuring Randomized controlled study, Multicenter, Prospective

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Complete rectal prolapse
  2. Informed consent
  3. Surgical correction is considered appropriate
  4. Capable to participate in follow-up visits and answering questionnaires

Exclusion Criteria:

-

Sites / Locations

  • Sahlgrenska University Hospital
  • Karlstad Central Hospital
  • Linköping University Hospital
  • Sunderbyn Hopsital
  • Skåne University Hospital
  • Vrinnevi Hospital
  • Danderyd Hospital
  • karolinska Univeristy Hospital Solna
  • Karolinska University Hospital Huddiinge
  • Sankt göran hospital
  • Uddevalla Hospital
  • Uppsala University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Abdominal suture rectopexy

Abdominal resection rectopexy

Perineal Delorme

Perineal Altemeier

Arm Description

Patients were randomized first into either an abdominal or a perineal approach. The abdominal group was then further randomized to suture rectopexy or resection rectopexy.

Patients were randomized first into either an abdominal or a perineal approach. The abdominal group was then further randomized to suture rectopexy or resection rectopexy.

Patients were randomized first into either an abdominal or a perineal approach. The perineal group was then further randomized to Delorme's operation or Altemeier's operation.

Patients were randomized first into either an abdominal or a perineal approach. The perineal group was then further randomized to Delorme's operation or Altemeier's operation.

Outcomes

Primary Outcome Measures

Bowel function
Wexner incontinence score, points, 0-20, higher worse result
Bowel function
Wexner incontinence score, points, 0-20, higher worse result
Bowel function
Wexner incontinence score, points, 0-20, higher worse result
Quality of Life
SF-36, points, 0-100 points, higher better result
Quality of Life
SF-36, points, 0-100 points, higher better result
Quality of Life
SF-36, points, 0-100 points, higher better result

Secondary Outcome Measures

Recurrence of rectal prolapse
recurrence at outpatient visits
Recurrence of rectal prolapse
recurrence at outpatient visits
Recurrence of rectal prolapse
recurrence at outpatient visits
Recurrence of rectal prolapse
Recurrence in Medical records

Full Information

First Posted
April 27, 2021
Last Updated
May 17, 2021
Sponsor
Danderyd Hospital
Collaborators
Uppsala University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04893642
Brief Title
Swedish Rectal Prolapse Trial
Official Title
To Resect or Not Resect - The Randomized Swedish Rectal Prolapse Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Terminated
Why Stopped
The study had planned to recruit 220 but was termianted in advance when 134 patients were randomized. This was done due to slow recruitment.
Study Start Date
March 23, 2000 (Actual)
Primary Completion Date
June 1, 2018 (Actual)
Study Completion Date
June 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Danderyd Hospital
Collaborators
Uppsala University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Rectal prolapse is a medical condition where rectum is protruding through the anal opening. The treatment is by surgery that can be performed with an anterior approach through the abdomen or a posterior perineal approach. The condition is more common in elderly patients and much more common in women compared to men. All used surgical techniques have advantages and disadvantages. The primary aim of this study is to evaluate if an abdominal or perineal surgical approach is best to correct a rectal prolapse. The outcome measures will be validated questionnaires on quality of Life (SF-36) and bowel function (modified Wexner incontinence score) as well as recurrence of the rectal prolapse and surgical complications. The study is a randomized multicenter trial with a 2x2 factorial design. Patients will be randomized between perineal and abdominal approach in a first randomization and the perineal group will then further be randomized into one of two specific operations (delorme or altemeier) and the abdominal group will be further randomized into suture rectopexy or resection rectopexy. The patients will be followed for 3 months, 1 year and 3 years and a longterm follow up of up to 17 years for recurrence.
Detailed Description
Background Full thickness rectal prolapse, or procidentia, is a benign but distressing condition. It is defined as the circumferential protrusion of all layers of the rectal wall through the anal sphincters. The annual incidence is 2,5 per 100 000, predominantly in the elderly, and male-to-female ratio is about 1:6. More than 100 different procedures have been described for surgical treatment of rectal prolapse and consensus has not yet been reached. Traditionally, perineal procedures have been reserved for older patients who are not fit for an abdominal operation. The two most common perineal procedures are Delorme's operation, i.e. mucosectomy and rectal plication, and perineal rectosigmoidectomy, also known as Altemeier's operation, which is a full-thickness excision of the rectum. The choices between abdominal vs. perineal approach and resection or not were all addressed in the Swedish rectal prolapse trial with possible differences in bowel function, quality of life, recurrence rate and complications as end points. Study design and randomization This was a multicenter randomized trial with a 2 x 2 factorial design conducted in 13 sites in Sweden. At inclusion, patients signed an informed consent form and the attending surgeon contacted the central trial office at the Danderyd Hospital, Stockholm, Sweden. Randomization was performed with randomly assigned envelopes, stratified for each participating center. Patients were randomized between perineal and abdominal approach (A). The perineal group was further randomized to Delorme's or Altemeier's procedure (B) and the abdominal group to suture rectopexy or resection rectopexy (C). Patients who were considered unsuitable for random allocation to a perineal or an abdominal procedure were included only in (B) or (C). Preoperative evaluation and procedures All patients were clinically examined and diagnosed with full thickness rectal prolapse. Further examinations with endoscopy, colon transit studies, anorectal manometry, defecography, endoanal ultrasound and pudendal nerve motor latency were optional and were performed as indicated at each surgeon's discretion. Operative procedures were described in the study protocol, see appendix. Abdominal procedures were performed laparoscopically or as open procedure. In order to validate data all questionnaires were gathered at the central trial hospital and inspected by a second researcher. The surgical procedures were identified and standardized to a large extent. Both minimal invasive and open surgery were allowed. For example the abdominal procedures were described that mobilization of rectum should be done in the posterior aspect, the lateral ligaments should not be divided, Suture rectopexy should be done with non-absorbable 0.0 sutures, the cul de sac should not be closed. The sample size was calculated to 220 patients in the first randomization between abdominal and perineal approach. With 220 patients a difference in recurrence of 13% could be identified with 90% power in a significance level of 5%. The plan was to analyze the categorical variables with either Fisher´s exact test or multivariate analysis. A main study office was situated at Danderyd Hospital and randomization was done from this office at the time when the patient was scheduled for surgery. All hospitals performing surgery for rectal prolapses in Sweden were invited to the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Prolapse
Keywords
Randomized controlled study, Multicenter, Prospective

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
This was a multicenter randomized trial with a 2 x 2 factorial design conducted in 13 sites in Sweden. Randomization was performed with randomly assigned envelopes, stratified for each participating center. Patients were randomized between perineal and abdominal approach (A). The perineal group was further randomized to Delorme's or Altemeier's procedure (B) and the abdominal group to suture rectopexy or resection rectopexy (C). Patients who were considered unsuitable for random allocation to a perineal or an abdominal procedure were included only in (B) or (C).
Masking
Outcomes Assessor
Masking Description
Masking was done for outcome assessor concerning the answers for questionnaires that were the primary endpoint. Masking of arms were not done concerning recurrence of rectal prolapse.
Allocation
Randomized
Enrollment
134 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Abdominal suture rectopexy
Arm Type
Active Comparator
Arm Description
Patients were randomized first into either an abdominal or a perineal approach. The abdominal group was then further randomized to suture rectopexy or resection rectopexy.
Arm Title
Abdominal resection rectopexy
Arm Type
Active Comparator
Arm Description
Patients were randomized first into either an abdominal or a perineal approach. The abdominal group was then further randomized to suture rectopexy or resection rectopexy.
Arm Title
Perineal Delorme
Arm Type
Active Comparator
Arm Description
Patients were randomized first into either an abdominal or a perineal approach. The perineal group was then further randomized to Delorme's operation or Altemeier's operation.
Arm Title
Perineal Altemeier
Arm Type
Active Comparator
Arm Description
Patients were randomized first into either an abdominal or a perineal approach. The perineal group was then further randomized to Delorme's operation or Altemeier's operation.
Intervention Type
Procedure
Intervention Name(s)
Suture rectopexy
Intervention Type
Procedure
Intervention Name(s)
resection rectopexy
Intervention Type
Procedure
Intervention Name(s)
Delorme's operation
Intervention Type
Procedure
Intervention Name(s)
Altemeier's operation
Primary Outcome Measure Information:
Title
Bowel function
Description
Wexner incontinence score, points, 0-20, higher worse result
Time Frame
3 months
Title
Bowel function
Description
Wexner incontinence score, points, 0-20, higher worse result
Time Frame
1 year
Title
Bowel function
Description
Wexner incontinence score, points, 0-20, higher worse result
Time Frame
3 years
Title
Quality of Life
Description
SF-36, points, 0-100 points, higher better result
Time Frame
3 months
Title
Quality of Life
Description
SF-36, points, 0-100 points, higher better result
Time Frame
1 year
Title
Quality of Life
Description
SF-36, points, 0-100 points, higher better result
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Recurrence of rectal prolapse
Description
recurrence at outpatient visits
Time Frame
3 months
Title
Recurrence of rectal prolapse
Description
recurrence at outpatient visits
Time Frame
1 year
Title
Recurrence of rectal prolapse
Description
recurrence at outpatient visits
Time Frame
3 years
Title
Recurrence of rectal prolapse
Description
Recurrence in Medical records
Time Frame
through study completion, an average of 12 years
Other Pre-specified Outcome Measures:
Title
Length of staý
Description
days
Time Frame
up to 30 days after surgical intervention
Title
Blood loss at operation
Description
milliliter
Time Frame
during the surgical procedure
Title
perioperative complications
Description
number classified by Clavien-Dindo
Time Frame
up to 30 days after surgical intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Complete rectal prolapse Informed consent Surgical correction is considered appropriate Capable to participate in follow-up visits and answering questionnaires Exclusion Criteria: -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fredrik Hjern, Ass Prof, MD
Organizational Affiliation
Danderyd Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Klas Pekkari, Md PhD
Organizational Affiliation
Danderyd Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Sahlgrenska University Hospital
City
Gothenburg
Country
Sweden
Facility Name
Karlstad Central Hospital
City
Karlstad
Country
Sweden
Facility Name
Linköping University Hospital
City
Linköping
Country
Sweden
Facility Name
Sunderbyn Hopsital
City
Luleå
Country
Sweden
Facility Name
Skåne University Hospital
City
Malmö
Country
Sweden
Facility Name
Vrinnevi Hospital
City
Norrköping
Country
Sweden
Facility Name
Danderyd Hospital
City
Stockholm
ZIP/Postal Code
18150
Country
Sweden
Facility Name
karolinska Univeristy Hospital Solna
City
Stockholm
Country
Sweden
Facility Name
Karolinska University Hospital Huddiinge
City
Stockholm
Country
Sweden
Facility Name
Sankt göran hospital
City
Stockholm
Country
Sweden
Facility Name
Uddevalla Hospital
City
Uddevalla
Country
Sweden
Facility Name
Uppsala University Hospital
City
Uppsala
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26599079
Citation
Tou S, Brown SR, Nelson RL. Surgery for complete (full-thickness) rectal prolapse in adults. Cochrane Database Syst Rev. 2015 Nov 24;2015(11):CD001758. doi: 10.1002/14651858.CD001758.pub3.
Results Reference
background
PubMed Identifier
16259169
Citation
Kairaluoma MV, Kellokumpu IH. Epidemiologic aspects of complete rectal prolapse. Scand J Surg. 2005;94(3):207-10. doi: 10.1177/145749690509400306.
Results Reference
background
PubMed Identifier
15655208
Citation
Madiba TE, Baig MK, Wexner SD. Surgical management of rectal prolapse. Arch Surg. 2005 Jan;140(1):63-73. doi: 10.1001/archsurg.140.1.63.
Results Reference
background
PubMed Identifier
28404199
Citation
Lundby L, Iversen LH, Buntzen S, Wara P, Hoyer K, Laurberg S. Bowel function after laparoscopic posterior sutured rectopexy versus ventral mesh rectopexy for rectal prolapse: a double-blind, randomised single-centre study. Lancet Gastroenterol Hepatol. 2016 Dec;1(4):291-297. doi: 10.1016/S2468-1253(16)30085-1. Epub 2016 Oct 4.
Results Reference
background
PubMed Identifier
23461778
Citation
Senapati A, Gray RG, Middleton LJ, Harding J, Hills RK, Armitage NC, Buckley L, Northover JM; PROSPER Collaborative Group. PROSPER: a randomised comparison of surgical treatments for rectal prolapse. Colorectal Dis. 2013 Jul;15(7):858-68. doi: 10.1111/codi.12177.
Results Reference
background
PubMed Identifier
29757320
Citation
Orwelius L, Nilsson M, Nilsson E, Wenemark M, Walfridsson U, Lundstrom M, Taft C, Palaszewski B, Kristenson M. The Swedish RAND-36 Health Survey - reliability and responsiveness assessed in patient populations using Svensson's method for paired ordinal data. J Patient Rep Outcomes. 2017;2(1):4. doi: 10.1186/s41687-018-0030-0. Epub 2018 Feb 7.
Results Reference
background
PubMed Identifier
35045155
Citation
Smedberg J, Graf W, Pekkari K, Hjern F. Comparison of four surgical approaches for rectal prolapse: multicentre randomized clinical trial. BJS Open. 2022 Jan 6;6(1):zrab140. doi: 10.1093/bjsopen/zrab140.
Results Reference
derived

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Swedish Rectal Prolapse Trial

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