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OpenTrials
Completed

NCT Number: NCT01676051

Surgical Prep in Hand Surgery

The purposes of this study are to identify the common bacterial flora on the hand and evaluate the efficacy of readily available skin-preparation solutions in the elimination of bacterial pathogens from the surgical site following skin preparation. The null hypothesis is that there is no difference in the efficacy of Chloraprep, Duraprep, and betadine in pre-operative skin preparation in clean, elective hand surgery cases.

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Key information

Age range

18 year–89 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Montefiore Hospital, Pittsburgh, Pennsylvania, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • the following procedures (carpal tunnel release, trigger finger release, cyst excision, 1st dorsal compartment release)

Exclusion criteria

  • prisoners
  • pregnant women

Treatment and study plan

Skin culture

Other

Culture swab used to culture skin adjacent to incision

Primary outcomes

  1. Number of positive cultures

    Time frame: after skin prep solution has dried

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Registry information

Official study title

Efficacy of Surgical Preparation Solutions in Hand Surgery

Important dates

Study start
2012
Primary completion
2014
Study completion
2017
First posted
Aug 30, 2012
Registry last updated
Oct 31, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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