Trial Outcomes & Findings for Chlorhexidine Drying Time (NCT NCT02095535)

Results Overview

Length of drying time from when Chloraprep solution is applied to skin to when skin is deemed dry.

Recruitment status

COMPLETED

Target enrollment

20 participants

Primary outcome timeframe

At Chloraprep application

Results posted on

2017-08-07

Participant milestones
Measure	Study Group All study participants Chlorhexidine gluconate: antiseptic
Recruitment STARTED	20
Recruitment COMPLETED	18
Recruitment NOT COMPLETED	2
Analysis STARTED	18
Analysis COMPLETED	18
Analysis NOT COMPLETED	0

Reasons for withdrawal
Measure	Study Group All study participants Chlorhexidine gluconate: antiseptic
Recruitment Protocol Violation	2

Race and Ethnicity were not collected from any participant.

Baseline characteristics by cohort
Measure	Study Group n=18 Participants All study participants Chlorhexidine gluconate: antiseptic
Age, Categorical <=18 years	0 Participants n=18 Participants
Age, Categorical Between 18 and 65 years	18 Participants n=18 Participants
Age, Categorical >=65 years	0 Participants n=18 Participants
Sex: Female, Male Female	18 Participants n=18 Participants
Sex: Female, Male Male	0 Participants n=18 Participants
Region of Enrollment Canada	18 participants n=18 Participants

Timeframe: At Chloraprep application

Length of drying time from when Chloraprep solution is applied to skin to when skin is deemed dry.

Outcome measures
Measure	Study Group n=18 Participants All study participants Chlorhexidine gluconate: antiseptic
Length of Drying Time	123 seconds Standard Deviation 32

Serious events: 0 serious events

Other events: 0 other events

Deaths: 0 deaths

Adverse event data not reported

Adverse event data not reported

UBC Department of Anesthesia - BC Women's Hospital

Phone: 604-875-2158