Role of Hyaluronic Acid in the Prevention of Post-operative Adhesions: a RCT (HiB)
Primary Purpose
Post Operative Adhesions
Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Hyaluronic Acid
NORMAL SALINE
Sponsored by
About this trial
This is an interventional treatment trial for Post Operative Adhesions
Eligibility Criteria
Inclusion Criteria:
- All consenting patients between the ages of 12-80, who undergo exploratory laparotomy and stoma formation
Exclusion Criteria:
Previous history of abdominal surgery History of peritoneal dialysis Patients in whom permanent stoma is formed
-
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
HiB
Normal saline
Arm Description
This group will receive the compound for the reduction of adhesions
This group will just receive normal saline to ensure blinding.
Outcomes
Primary Outcome Measures
POST OPERATIVE ADHESIONS TO BE EVALUATED BY LAPAROSCOPY AT THREE MONTHS INTERVAL
Secondary Outcome Measures
Full Information
NCT ID
NCT02790177
First Posted
May 23, 2016
Last Updated
May 29, 2016
Sponsor
Services Institute of Medical Sciences, Pakistan
1. Study Identification
Unique Protocol Identification Number
NCT02790177
Brief Title
Role of Hyaluronic Acid in the Prevention of Post-operative Adhesions: a RCT
Acronym
HiB
Official Title
Is Hyaluronic Acid Effective in the Prevention of Post-operative Adhesion?
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Unknown status
Study Start Date
June 2016 (undefined)
Primary Completion Date
May 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Services Institute of Medical Sciences, Pakistan
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The objective of study is to determine the effect of hyaluronic acid on the formation of post-operative adhesions. It will be a randomized control trial comparing the product against normal saline.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Operative Adhesions
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
HiB
Arm Type
Experimental
Arm Description
This group will receive the compound for the reduction of adhesions
Arm Title
Normal saline
Arm Type
Placebo Comparator
Arm Description
This group will just receive normal saline to ensure blinding.
Intervention Type
Drug
Intervention Name(s)
Hyaluronic Acid
Intervention Type
Drug
Intervention Name(s)
NORMAL SALINE
Primary Outcome Measure Information:
Title
POST OPERATIVE ADHESIONS TO BE EVALUATED BY LAPAROSCOPY AT THREE MONTHS INTERVAL
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
- All consenting patients between the ages of 12-80, who undergo exploratory laparotomy and stoma formation
Exclusion Criteria:
Previous history of abdominal surgery History of peritoneal dialysis Patients in whom permanent stoma is formed
-
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Role of Hyaluronic Acid in the Prevention of Post-operative Adhesions: a RCT
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