Bleeding in Laser Haemorrhoidoplasty
Comparison of Post-operative Bleeding Incidence in Laser Haemorrhoidoplasty Versus Laser Haemorrhoidoplasty With Haemorrhoidal Artery Ligation: A Double-Blinded Randomized Controlled Trial
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Kuala Lumpur, Malaysia, 50603
- University of Malaya
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged 18 and above
- Diagnosed with symptomatic haemorrhoid
- Able to give informed consent
- Fit to undergo anaesthesia
- Agreeable for randomization and shows no preference for either group
Exclusion Criteria:
- Have stated a preference toward a certain treatment option
- Haemorrhoid condition requiring emergency surgery
- Haemorrhoids condition associated with other anorectal pathology such as fistula in ano, perianal abcess, and anal fissure
- Unable to provide informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
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Experimental: Laser Haemorrhoidoplasty
A stab incision was made at the ano-cutaneous junction and the anodermis was tunneled with artery forceps to the pedicle of the haemorrhoids.
The laser catheter was introduced submucosally towards the pedicle guided by a visible beam to ascertain the exact location of the laser fibre.
This was then followed by about six pulsed laser energy delivered at five mm interval, while gradually withdrawing the laser catheter.
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Post-operatively, all subjects were given tablet Paracetamol 1 gm six hourly and Capsule Celecoxib 200 mg 12 hourly as pain control for five days.
They were given Syrup Lactulose 15 cc 12 hourly for one week to prevent constipation.
Subjects were discharged on the same day or one day after surgery.
All patients were assessed in the clinic by a nurse/medical officer blinded to the type of procedure performed on post-operative 24 hours, one week and six weeks.
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Experimental: Haemorrhoidal Artery Ligation
In addition to the delivery of laser energy as per the procedure described above, each identified pedicle was ligated with a suture, without Doppler guidance.
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Post-operatively, all subjects were given tablet Paracetamol 1 gm six hourly and Capsule Celecoxib 200 mg 12 hourly as pain control for five days.
They were given Syrup Lactulose 15 cc 12 hourly for one week to prevent constipation.
Subjects were discharged on the same day or one day after surgery.
All patients were assessed in the clinic by a nurse/medical officer blinded to the type of procedure performed on post-operative 24 hours, one week and six weeks.
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What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Overall post-operative bleeding incidence
Time Frame: One day
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The assessment was made using of bleeding using verbal rating scale and Clavien-Dindo score.
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One day
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Overall post-operative bleeding incidence
Time Frame: One week
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The assessment was made using of bleeding using verbal rating scale and Clavien-Dindo score.
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One week
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Overall post-operative bleeding incidence
Time Frame: Six weeks
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The assessment was made using of bleeding using verbal rating scale and Clavien-Dindo score.
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Six weeks
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pain score
Time Frame: One day
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The assessment was made using the visual analogue scale (VAS)
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One day
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Pain score
Time Frame: One week
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The assessment was made using the visual analogue scale (VAS)
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One week
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Pain score
Time Frame: Six weeks
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The assessment was made using the visual analogue scale (VAS)
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Six weeks
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The presence of perianal swelling
Time Frame: One day
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The assessment was documented as its presence or the absence
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One day
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The presence of perianal swelling
Time Frame: One week
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The assessment was documented as its presence or the absence
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One week
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The presence of perianal swelling
Time Frame: Six weeks
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The assessment was documented as its presence or the absence
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Six weeks
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Operation time
Time Frame: Day 0
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The assessment was made based on the clinical records
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Day 0
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Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Shu Yu Lim, MSurg, University of Malaya
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- NMRR-15-1112-24065
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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