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Clinical Trials/NCT00735605
NCT00735605CompletedNot Applicable

Comparative Study Between Surgical and Non Surgical Treatment of Anismus in Patients With Symptoms of Obstructed Defecation

Mansoura University1 site in 1 country60 target enrollmentStarted: September 1, 2006Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
improvement in bowel habit (regarding the straining severity, anorectal pain,number of weakly bowel movement,sensation of incomplete defecation and need of digitation or enema and using constipation score)

Study Overview

Brief Summary

Comparative study between surgical and non surgical treatment of anismus in patients with symptoms of obstructed defecation.

Anismus is a significant cause of chronic constipation. This study came to compare the results of BFB training , BTX-A injection and PDPR in the treatment of anismus patients. Patients and methods: Seventy two anismus patients fulfilled Rome II criteria for functional constipation were included in this study. All patients underwent anorectal manometry, balloon expulsion test, defecography, and electromyography activity of the EAS. All patients had non relaxing puborectalis muscle.. The patients were randomized into three groups. Group I patients received biofeedback therapy, two times per week for about 1 month. Group II patients were injected with BTX- A. Group 111 partial division of puborectalis was done. Follow up was conducted weekly in the first month then monthly for about 1 year.

Detailed Description

Key words:

Obstructed defecation, chronic constipation, puborectalis, pelvic floor

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 69 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •60patients fulfilled Rome II criteria for functional constipation
  • •All patients were unresponsive to laxatives or enema use

Exclusion Criteria

  • •Pregnant patients
  • •Patients with sphincteric defect
  • •Any patient proved to have colonic inertia by colon transit time
  • •Any patient with previous history of pelvic surgery e.g. mesh rectopexy
  • •Duhamel operation were excluded

Arms & Interventions

2 BTX A

Active Comparator

Injected with BTX-A in the left lateral position; anesthesia was not required

Intervention: BTX A (Other)

3: PDPR

Active Comparator

Inner half of puborectalis sling was divided on each side by using a scalpel NO

Intervention: PDPR (Procedure)

1:BFD

Active Comparator

The investigators used pressure based biofeedback training, using a perfused eight-channel polyvinyl catheter with a compliant balloon at the tip

Intervention: BFD (Other)

Outcomes

Primary Outcomes

improvement in bowel habit (regarding the straining severity, anorectal pain,number of weakly bowel movement,sensation of incomplete defecation and need of digitation or enema and using constipation score)

Time Frame: 1 year

Secondary Outcomes

  • per rectal examination,manometeric relaxation,balloon expulsion,defecogram,EMG examination of anal sphincter to monitor any change in paradoxical contraction,recurrences,incontinence,complication(1 year)

Investigators

Sponsor Class
Other

Study Sites (1)

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