Clinical Trials Directory

Trials / Completed

CompletedNCT00738543

Povidone-iodine Against Sodium Hypochlorite as Skin Antiseptics

Comparative Study of 10% Povidone-iodine Against 10% Sodium Hypochlorite as Skin Antiseptics in Human Volunteers.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Universidad de Guanajuato · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The investigators have few options for skin antisepsis. Alternatives for povidone-iodine, which is the most commonly used agent, are costly or ineffective. To have more options, this study is needed. The investigators want to know if there are difference between the use of 10% sodium hypochlorite or 10% povidone-iodine for skin antisepsis.

Detailed description

Sodium hypochlorite at 10% has been widely used as antiseptic in patients on dialysis as well as for irrigation of wounds and burns. Since it has been used successfully in caring for the exit site of hemodialysis catheters, it is reasonable to propose its use for the insertion and care of central intravascular catheters, as well as for skin preparation before surgery. Alternatives for povidone-iodine, which is the agent most commonly used, are costly or ineffective. To have more options, this study is needed to know if 10% sodium hypochlorite is similar to the most common option for skin antisepsis.

Conditions

Interventions

TypeNameDescription
OTHERWHOLE GROUP OF 48 VOLUNTEERSTwo antiseptics (10% povidone iodine and 10% sodium hypochlorite) and one control were tested as skin antiseptics. The intervention consisted of preparing the skin with the antiseptic or the control. The areas were approximately 25 cm2 on the forearm for each antiseptic or control. The antiseptic or control were applied in an outward circular motion using a swab that was soaked with the solution. The solution was then kept on the skin for 60 seconds before the bacterial culture was conducted. All volunteers were instructed to continue the use of neutral soap and shampoo without antiseptics during the follow-up period.

Timeline

Start date
2008-08-01
Primary completion
2008-12-01
Completion
2008-12-01
First posted
2008-08-20
Last updated
2013-06-24
Results posted
2010-08-17

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT00738543. Inclusion in this directory is not an endorsement.