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High Dose Multiple Site Injection of Botox Versus Lateral Sphincterotomy in Chronic Analfissure (professor)

Primary Purpose

Chronic Anal Fissure

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
botox injection in intersphincteric space
lateral internal sphincterotomy
Sponsored by
Zagazig University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Anal Fissure

Eligibility Criteria

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

Inclusion Criteria:

  • patients suffering chronic anal fissure aged above 16 years old

Exclusion Criteria:

  • those with previous anal surgery,
  • complicated anal fissure,
  • unfit for surgery,
  • specific disease as Crohn's disease and ulcerative colitis,
  • malignancy,
  • anal fistula or abscess
  • those with systemic disease requiring treatment with calcium channel blockers and /or nitrates

Sites / Locations

  • Zagazig Faculty of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

group 1 botox group

group 2 lateral sphincterotomy group

Arm Description

48 patients subjected to 80 IU botox injection under GAin lithotomy position in the 5,7,11, and 1 O'clock positions

48 patients subjected to lateral internal sphincterotomy under GAin lithotomy position

Outcomes

Primary Outcome Measures

complete healing of fissure
complete epithelialization of the floor of the chronic anal wound achieved through clinical examination at follow up visits
loss of anal continence
inability to control stool or flatus measured by modified wexner score questionaire
recurrence
the anal fissure reformed again after complete healing measured by clinical examination

Secondary Outcome Measures

time taken for complete healing
time taken for complete epithelialization of the anal wound measured by clinical examination
post operative pain
pain in the postoperative time measured by visual analogue scale

Full Information

First Posted
November 14, 2019
Last Updated
November 19, 2019
Sponsor
Zagazig University
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1. Study Identification

Unique Protocol Identification Number
NCT04166175
Brief Title
High Dose Multiple Site Injection of Botox Versus Lateral Sphincterotomy in Chronic Analfissure
Acronym
professor
Official Title
Treatment of Chronic Anal Fissure, Lateral Internal Sphincterotomy Versus Local Injection of High Dose Botulinum Toxin: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
May 30, 2019 (Actual)
Study Completion Date
May 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zagazig University

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
comparison between the effect of lateral sphincterotomy against high dose botox injection in chronic anal fissure the outcome was healing time, recurrence continence relapse pain pruritus
Detailed Description
This randomized comparative clinical trial was carried out over 2 year in the period between January 2018 and December 2019 on total number of 96 patients suffering chronic anal fissure the participants were randomly allocated into two groups each 48 patients ; group (1) the botulinum ( Botox) group, they were subjected to 80 IU Botox injection as an intervention for treatment of chronic anal sphincter, and group 2 the sphincterotomy group, underwent internal sphincterotomy as a surgical intervention for treatment of chronic anal fissure. The study was approved by the institutional review board and the local ethical committee of our university hospital The condition of the current study is chronic anal fissure defined as the presence of anterior or posterior chronic anal wound with skin tag at its lower end and hypertrophied anal papilla at its upper end with induration around its edges in patients complaining of anal pain, constipation, and/or fresh anal bleeding for at least two months. Randomization was achieved using computer generated cards. Inclusion criteria; patients suffering chronic anal fissure aged above 16 years old Exclusion criteria; those with previous anal surgery, complicated anal fissure, unfit for surgery, specific disease as Crohn's disease and ulcerative colitis, malignancy, anal fistula or abscess those with systemic disease requiring treatment with calcium channel blockers and /or nitrates Patients of both groups were subjected to thorough history taking, clinical examination, digital rectal examination and anorectal manometry for diagnosis of chronic anal fissure and exclusion of any other anal condition and incontinence, patient signed an informed written consent, routine preoperative investigations performed as usual. Interventions; Botulinum toxin (Botox) injection; was performed under general anesthesia in the lithotomy position, where 80 IU of Botox was injected in four positions each 20 IU namely in 5, 7, 11, and 1 O'clock positions in the intersphincteric space not deeper than the midpoint of the anal canal. Lateral internal sphincterotomy; was performed under general anesthesia where the lower part of the internal sphincter was cut by electrocautery on the left lateral position to an extent not beyond the proximal end of the fissure, the sentinel pile was also removed. After the procedure patients were advised for bulking agents, stool softener, and sitz baths The follow up was carried out in the outpatient clinic by the attending surgeon (not a study participant) after 1 week then 1, 2, 3, 6, 9 and 12 months post-procedure. The primary outcome of the current study is complete healing of the chronic anal fissure, recurrence in the follow up time, and development of incontinence, incontinence is described as in (the Cleveland Clinic Florida-Fecal Incontinence (CCF-FI) scoring system), which contains 5 questions on solid and liquid stool leakage, gas leakage, pad use, and lifestyle restriction. the secondary outcome is postoperative or post-injection pain measured by visual analogue scale (VAS) and the time taken for complete healing of fissure (defined as complete epithelialization of the fissure). Demographic data, presentation data, follow up data including primary and secondary outcome all collected and analyzed properly using t test, chi square test, and Z test in SPSS program 22 version.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Anal Fissure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
two groups of patients randomly allocated group1 the botox group received 80 IU botox injection and group 2 under went lateral internal sphincterotomy
Masking
Participant
Masking Description
participant don't know the procedure
Allocation
Randomized
Enrollment
96 (Actual)

8. Arms, Groups, and Interventions

Arm Title
group 1 botox group
Arm Type
Active Comparator
Arm Description
48 patients subjected to 80 IU botox injection under GAin lithotomy position in the 5,7,11, and 1 O'clock positions
Arm Title
group 2 lateral sphincterotomy group
Arm Type
Active Comparator
Arm Description
48 patients subjected to lateral internal sphincterotomy under GAin lithotomy position
Intervention Type
Procedure
Intervention Name(s)
botox injection in intersphincteric space
Intervention Description
injection of 80 IU of botox in the intersphincteric space in 5,7,11 and 1 O'clock position
Intervention Type
Procedure
Intervention Name(s)
lateral internal sphincterotomy
Intervention Description
lateral internal sphincterotomy under GA in lithotomy position
Primary Outcome Measure Information:
Title
complete healing of fissure
Description
complete epithelialization of the floor of the chronic anal wound achieved through clinical examination at follow up visits
Time Frame
2 months
Title
loss of anal continence
Description
inability to control stool or flatus measured by modified wexner score questionaire
Time Frame
1 week
Title
recurrence
Description
the anal fissure reformed again after complete healing measured by clinical examination
Time Frame
1 year
Secondary Outcome Measure Information:
Title
time taken for complete healing
Description
time taken for complete epithelialization of the anal wound measured by clinical examination
Time Frame
1 year
Title
post operative pain
Description
pain in the postoperative time measured by visual analogue scale
Time Frame
1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients suffering chronic anal fissure aged above 16 years old Exclusion Criteria: those with previous anal surgery, complicated anal fissure, unfit for surgery, specific disease as Crohn's disease and ulcerative colitis, malignancy, anal fistula or abscess those with systemic disease requiring treatment with calcium channel blockers and /or nitrates
Facility Information:
Facility Name
Zagazig Faculty of Medicine
City
Zagazig
State/Province
Sharqya
ZIP/Postal Code
44519
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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High Dose Multiple Site Injection of Botox Versus Lateral Sphincterotomy in Chronic Analfissure

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