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NCT00524888 Clinical Trial

Suturing vs Biological Adhesive in Simple Lacerations of Hand

Lacerations Clinical Trial

— sutvsglu  

Official title:
Suturing Vs Adhesion for Hand Lacerations in the ER A Randomized Prospective Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT00524888
Other study ID # sutvsglu-HMO-CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 4, 2007
Last updated September 4, 2007
Start date September 2007

Study information
Verified date August 2007
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

To assess the difference in clinical outcome between lacerations in the hand treated by sutures versus treated by tissue adhesive.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 200
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Any age

- Hand laceration distal to the volar wrist crease.

Exclusion Criteria:

- Fracture , tendon, artery involvement, more than 8 hours from laceration to trx,

- Immunosuppression

- Anticoagulation therapy

- Diabetes

- Unable to achieve homeostasis in more than 15 minutes

- Unwilling to participate in the study

- Unable to participate in the follow up or bite of any kind.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• suturing laceration
suturing simple lacerations of the hand
• bioadhesive
using bioadhesive on simple lacerations of the hand

Locations
Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (1)
Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Wound appearance 3 Months
Secondary pain of treatment and time length of treatment 3 months
See also
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Completed NCT02618772 - Intranasal Midazolam for Treatment of Anxiety in Children Undergoing Suturing in the Pediatric Emergency Department Phase 4
Completed NCT01053637 - Pain and Anxiety Management With Oral Narcotic for Pediatric Suture Repair N/A
Recruiting NCT01925898 - A Randomized, Clinical Trial of Oral Midazolam Versus Oral Ketamine for Sedation During Laceration Repair. Phase 4
Completed NCT00547638 - Study to Show Equivalence of DERMABOND PROTAPE to DERMABOND HVD for Wound Closure Phase 2
Completed NCT01202487 - Gluing Lacerations Utilizing Epinephrine Phase 2
Withdrawn NCT00933829 - Comparison of Cosmetic Outcomes of Lacerations Repaired Using Absorbable Versus Non-absorbable Sutures N/A
Completed NCT00681070 - Cosmetic Outcomes of Absorbable Versus Non-absorbable Sutures in Pediatric Facial Lacerations N/A
Recruiting NCT03830515 - Evaluation of microMend Device to Close Lacerations N/A