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Suture Versus Glue (Dermabond) Closure During Cesarean Delivery

NCT02831946 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2016-07-13

No results posted yet for this study

Summary

To investigate the effect of intracutaneous suture closure versus Glue (dermabond) closure at cesarean section (CS) on long-term cosmetic and maternal outcome.

Conditions

  • Adhesive; Band
  • Suture; Complications

Interventions

DEVICE

MODIFIED VICRYL PLUS

closing the intra-cuticular layer with MODIFIED VICRYL PLUS suture

DEVICE

DERMABOND GLUE

closing the intra-cuticular layer with Dermabond glue

Sponsors & Collaborators

  • Meir Medical Center

    lead OTHER

Principal Investigators

  • Reut Ohana · Meir Helsinki

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2017-05-31
Completion
2018-02-28

Countries

  • Israel

Study Locations

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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 NCT02831946 on ClinicalTrials.gov