Clinical Trials Directory

Trials / Unknown

UnknownNCT03014778

Efficacy of Two Vaginal Solutions in Preoperative Use

Efficacy Comparison of Two Vaginal Solutions for Preoperative Use in Candidate Women for Vaginal Surgeries

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
HaEmek Medical Center, Israel · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

This study is necessary in order to provide proof the effectiveness of Chlorhexidine gluconate and its safety.

Detailed description

It is well known from the literature that the use of Povidone-iodone based solution for vaginal preparation before surgery is fraught with side effects and sensitivity, and often does not provide sufficient eradication of colonies of pathogens from the operation field. It is also known that Chlorhexidine gluconate in low concentration provides a better result and does not cause side effects more than Povidone-iodone, but the chlorhexidine is still not approved for washing the mucous membranes. This study is necessary in order to provide proof of its effectiveness and safety.

Conditions

Interventions

TypeNameDescription
DRUGThe Chlorhexidine gluconate 0.05%Washing vagina pre- operatively with Chlorhexidine gluconate 0.05%
DRUG10% Povidone iodineWashing vagina pre- operatively with 10% Povidone iodine

Timeline

Start date
2017-01-01
Primary completion
2018-12-31
Completion
2019-03-01
First posted
2017-01-09
Last updated
2018-02-28

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT03014778. Inclusion in this directory is not an endorsement.