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Vaginal Preparation Prior to Hysterectomy

NCT03412734 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 94

Last updated 2021-01-11

Study results available
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Summary

This is a randomized controlled trial to determine the influence of chlorhexidine gluconate surgical/topical antiseptic solutions on the bacterial environment of the vagina during hysterectomy and compare that to the effect of standard iodine-based preparations on the same.

Conditions

  • Hysterectomy

Interventions

DRUG

Chlorhexidine

Chlorhexidine preparation solutions

DRUG

Iodine

Iodine-based preparation solutions

Sponsors & Collaborators

  • TriHealth Inc.

    lead OTHER

Principal Investigators

  • Catrina Crisp, MD · TriHealth - Cincinnati Urogynecology Associates

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-18
Primary Completion
2019-08-26
Completion
2020-01-29
FDA Drug
Yes

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 NCT03412734 on ClinicalTrials.gov