CTRI/2025/04/085081Not yet recruitingPhase 1
COMPARISON OF N-BUTYL 2 CYANOACRYLATE TISSUE ADHESIVE AND NYLON SUTURES IN EXTRAORAL MAXILLOFACIAL LACERATIONS AND INCISIONS – A RANDOMISED CONTROLLED SINGLE CENTERED TRIAL
Abdulla Noor M1 site in 1 country44 target enrollmentStarted: April 30, 2025Last updated:
Trial Snapshot
- Phase
- Phase 1
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 44
- Locations
- 1
- Primary Endpoint
- cyanoacrylate tissue adhesive reduces operative time
Study Overview
Brief Summary
The study is done to compare the efficacy of cyanoacrylate skin glue with nylon sutures on facial lacerations and incisions and note its inflammatory and aesthetic outcomes post operatively.
Study Design
- Study Type
- Interventional
- Allocation
- Adaptive randomization, such as minimization
- Masking
- Double Blind Double Dummy
Eligibility Criteria
- Ages
- 18.00 Year(s) to 70.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Age group is selected between 15 and 70 years Lacerations should be within 5 cm length Both sexes are included in the study Patients who turn up for post operative evaluation Clean, non contaminated lacerated wounds Wounds of depth not more than 2 cm.
Exclusion Criteria
- •Medically compromised patients Lacerations which require to be closed under tension Decubitus ulcer, crushed wounds and severe abrasions Known person with family history of keloid or hypertrophied scar formation.
Outcomes
Primary Outcomes
cyanoacrylate tissue adhesive reduces operative time
Time Frame: immediate post operatively,3rd day, 7th day, 1 week, 2 weeks and i month post operatively
Secondary Outcomes
- good hemostatic property(immediate post operatively,3rd day, 7th day, 1 week, 2 weeks & 1 month post operatively)
Investigators
Study Sites (1)
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