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Interrupted Oblique Intradermal Suture Versus Conventional Interrupted Intradermal Suture

NCT03001856 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 144

Last updated 2017-01-10

No results posted yet for this study

Summary

This study was conducted to demonstrate the equivalence of wound outcomes between the interrupted oblique intradermal suture (OIS) and conventional interrupted intradermal suture (IS) methods

Conditions

  • Surgery

Interventions

PROCEDURE

Oblique Intradermal Suture

PROCEDURE

Intradermal Suture

Sponsors & Collaborators

  • Mae Fah Luang University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2016-12-31
Completion
2016-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03001856 on ClinicalTrials.gov