RCT Comparing Conventional Haemorrhoidectomy With Laser Haemorrhoidoplasty (COHLAH)
Primary Purpose
Hemorrhoids
Status
Recruiting
Phase
Phase 2
Locations
Singapore
Study Type
Interventional
Intervention
Laser Haemorrhoidoplasty (LAH)
Open milligan-morgan conventional haemorrhoidectomy
Sponsored by
About this trial
This is an interventional treatment trial for Hemorrhoids focused on measuring haemorrhoid, laser, haemorrhoidectomy
Eligibility Criteria
Inclusion Criteria:
- between 21-90 years old
- presents with symptomatic haemorrhoids as evident from clinical assessment
- never had any haemorrhoid-related operations performed on them before
- fit for general anaesthesia
- able to give informed consent
- willing to be randomized
- willing to fill in post-operative questionnaires and be compliant to follow up
Exclusion Criteria:
- Are pregnant
- Are prisoners
- Intellectually, mentally or emotionally deemed not able to provide an informed consent and/or are unable to fill up the post-procedure questionnaires/VAS score
- Have had previous haemorrhoid procedural treatment before (except Rubber Band Ligation)
- Declined endoscopic evaluation
- Are on anti-coagulation
- Have history of thrombophilia
- Are on steroids
- Have haemorrhoids which are incidentally found on endoscopy/clinical examination but are asymptomatic from it
Sites / Locations
- Sengkang General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Laser Haemorrhoidoplasty (LAH)
Conventional Open Haemorrhoidectomy (COH)
Arm Description
treatment that we would like to study
gold standard treatment as comparator
Outcomes
Primary Outcome Measures
Pain scores
Daily visual analogue pain scale in the first 10 days after surgery. A score of 10 being the worst pain experienced and 1 being no pain experienced.
Secondary Outcome Measures
Operative duration
duration of operation
Post-op bleeding
incidence of bleeding post op
readmission
readmission due to complications
recurrence
recurrence of haemorrhoids or symptoms
Quality of Life measures
2 validated questionnaires will be used ([patient self reported symptoms of haemorrhoids] Nystrom, et al. and [standardised haemorrhoidectomy QOL survey] Chew, et al)
Full Information
NCT ID
NCT04329364
First Posted
March 19, 2020
Last Updated
April 10, 2023
Sponsor
Sengkang General Hospital
Collaborators
Biolitec
1. Study Identification
Unique Protocol Identification Number
NCT04329364
Brief Title
RCT Comparing Conventional Haemorrhoidectomy With Laser Haemorrhoidoplasty
Acronym
COHLAH
Official Title
A Randomised Controlled Trial Comparing Conventional Open Haemorrhoidectomy and Laser Haemorrhoidoplasty in the Treatment of Symptomatic Haemorrhoids: COHLAH Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sengkang General Hospital
Collaborators
Biolitec
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Haemorrhoids or piles are the most common colorectal condition in the local population. Patients often present with bleeding with bowel movement or anal discomfort, both of which causes significant anxiety and stress. For symptomatic sizeable piles, the treatment of choice still remains the conventional open excision (COH). However, this technique carries with it a significant risk of bleeding and pain immediately after the operation, leading to some period of discomfort for the patients. The laser haemorrhoidoplasty procedure (LAH) has been shown in preliminary studies to have less pain, and less complications compared to COH. This study aims to directly compare these two techniques in a local Asian population.
The investigators would be conducting a single-centre RCT simultaneously comparing the conventional open Milligan-Morgan haemorrhoidectomy (COH) and the laser haemorrhoidoplasty procedure (LAH) for the treatment of symptomatic grade ll-lV haemorrhoids. Primary outcomes will be post-operative pain while secondary outcomes include post-operative bleeding, readmission and/or reoperations, haemorrhoid-related quality of life (QoL) results and recurrence of symptoms up to a year post procedure
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhoids
Keywords
haemorrhoid, laser, haemorrhoidectomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Model Description
The investigators would be conducting a single-centre RCT simultaneously comparing the conventional open Milligan-Morgan haemorrhoidectomy (COH) and the laser haemorrhoidoplasty procedure (LAH) for the treatment of symptomatic grade ll-lV haemorrhoids.
Masking
ParticipantOutcomes Assessor
Masking Description
Allocation is provided through calling the study administrator at time of Examination under Anaesthesia. Thus, the participant is blinded to the procedure. There will also be no cross-over from one study arm to another.
An independent research administrator, not part of the randomisation process, will also contact the patient 3 months and 1 year after the procedure as mentioned above.
Allocation
Randomized
Enrollment
128 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Laser Haemorrhoidoplasty (LAH)
Arm Type
Experimental
Arm Description
treatment that we would like to study
Arm Title
Conventional Open Haemorrhoidectomy (COH)
Arm Type
Active Comparator
Arm Description
gold standard treatment as comparator
Intervention Type
Combination Product
Intervention Name(s)
Laser Haemorrhoidoplasty (LAH)
Intervention Description
Using a laser diode to cause coagulative necrosis to the haemorrhoidal cushion
Intervention Type
Procedure
Intervention Name(s)
Open milligan-morgan conventional haemorrhoidectomy
Intervention Description
conventional excisional haemorrhoidectomy
Primary Outcome Measure Information:
Title
Pain scores
Description
Daily visual analogue pain scale in the first 10 days after surgery. A score of 10 being the worst pain experienced and 1 being no pain experienced.
Time Frame
10 days from op
Secondary Outcome Measure Information:
Title
Operative duration
Description
duration of operation
Time Frame
during operation
Title
Post-op bleeding
Description
incidence of bleeding post op
Time Frame
10 days from operation
Title
readmission
Description
readmission due to complications
Time Frame
3 months
Title
recurrence
Description
recurrence of haemorrhoids or symptoms
Time Frame
1 year post operation
Title
Quality of Life measures
Description
2 validated questionnaires will be used ([patient self reported symptoms of haemorrhoids] Nystrom, et al. and [standardised haemorrhoidectomy QOL survey] Chew, et al)
Time Frame
10 days, 1 month, 3 months and 1 year post operation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
between 21-90 years old
presents with symptomatic haemorrhoids as evident from clinical assessment
never had any haemorrhoid-related operations performed on them before
fit for general anaesthesia
able to give informed consent
willing to be randomized
willing to fill in post-operative questionnaires and be compliant to follow up
Exclusion Criteria:
Are pregnant
Are prisoners
Intellectually, mentally or emotionally deemed not able to provide an informed consent and/or are unable to fill up the post-procedure questionnaires/VAS score
Have had previous haemorrhoid procedural treatment before (except Rubber Band Ligation)
Declined endoscopic evaluation
Are on anti-coagulation
Have history of thrombophilia
Are on steroids
Have haemorrhoids which are incidentally found on endoscopy/clinical examination but are asymptomatic from it
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fung Joon Foo
Phone
+65 6930 5354
Email
foo.fung.joon@singhealth.com.sg
First Name & Middle Initial & Last Name or Official Title & Degree
Fung Joon Foo
Phone
+65 6930 6000
Email
foo.fung.joon@singhealth.com.sg
Facility Information:
Facility Name
Sengkang General Hospital
City
Singapore
ZIP/Postal Code
544886
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fung Joon Foo
Phone
+65 6930 5354
Email
foo.fung.joon@singhealth.com.sg
First Name & Middle Initial & Last Name & Degree
Frederick H Koh, FRCSEd
First Name & Middle Initial & Last Name & Degree
Min-Hoe Chew, FRCSEd
First Name & Middle Initial & Last Name & Degree
Winson Tan, FRCSEd
First Name & Middle Initial & Last Name & Degree
Sharmini Sivarajah, FRCSEd
First Name & Middle Initial & Last Name & Degree
Leonard Ho, FRCSEd
First Name & Middle Initial & Last Name & Degree
Fung Joon Foo, FRCSEd
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
country's personal data protection Act restrictions clearance
Citations:
PubMed Identifier
33631763
Citation
Koh FH, Foo FJ, Ho L, Sivarajah SS, Tan WJ, Chew MH. Study Protocol for the Use of Conventional Open Haemorrhoidectomy versus Laser Haemorrhoidoplasty in the Treatment of Symptomatic Haemorrhoids: A Randomized Controlled Trial. Eur Surg Res. 2020;61(6):201-208. doi: 10.1159/000513844. Epub 2021 Feb 25.
Results Reference
derived
Learn more about this trial
RCT Comparing Conventional Haemorrhoidectomy With Laser Haemorrhoidoplasty
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