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Study to Compare Suture Material in Closure of Uterine Incision in Cesarian Section

NCT02517710 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2018-08-10

No results posted yet for this study

Summary

Prospective single blinded trial comparing standard synthetic suture material to a synthetic barbed suture in closure of uterine incision, during Cesarean section procedures.

Conditions

  • Hysterotomy Closure

Interventions

PROCEDURE

Stratafix synthetic barbed suture

hysterotomy closure in Cesarian section

Sponsors & Collaborators

  • Russell J.Stankiewicz, MD

    collaborator UNKNOWN

  • Ob/GYN Associates of Evangelical Hospital

    collaborator UNKNOWN

  • The Commonwealth Medical College

    collaborator UNKNOWN

  • Nickolas Serniak, BS, MS 4

    collaborator UNKNOWN

  • Neil Cooper, MS, MS 4

    collaborator UNKNOWN

  • Jennifer L. MacDonald, PA

    collaborator UNKNOWN

  • Evangelical Community Hospital, Lewisburg, PA

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-04-30
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • United States

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 NCT02517710 on ClinicalTrials.gov