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NCT01097135 · ClinicalTrials.gov registry record · NA
Evaluating the Effectiveness of 2 Surgical Skin Preparation Methods in Reducing Surgical Wound Drainage After Total Hip or Knee Replacement
A NA study of Drainage, sponsored by Rothman Institute Orthopaedics.
- Completed
- Registry status
- NA
- Development phase
- 600
- Enrollment target
- 1
- Study location
NCT01097135 is a NA study of Drainage that has completed, run by Rothman Institute Orthopaedics. The registered enrollment target is 600 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01097135, a NA study of Drainage, has completed, sponsored by Rothman Institute Orthopaedics.
- COMPLETED
- Registry status
- NA
- Development phase
- 600 participants
- Enrollment target
- 1
- Study location
Study Summary
Surgical skin complications can be costly and could contribute to extended in-patient stay following total joint replacement or even the need for re-admission. If efficacy in reducing the incidence of post-operative wound drainage and, in turn, surgical wound complications can be demonstrated, it may also reduce the length of hospital stay and the need for revision surgery or readmission. The aim of this research is to investigate the incidence of post-operative wound drainage following elective total joint arthroplasty using two surgical skin preparation protocols.
Conditions Studied
Interventions
- DRUG Duraprep Surgical Solution
Study Locations (1)
Pennsylvania
- Rothman Institute - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 2010-03 |
| Est. Completion | 2012-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01097135
The ClinicalTrials.gov registry entry for NCT01097135 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rothman Institute Orthopaedics, which has 23 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Drainage appearing as the primary indexed condition, and to 1 intervention - of which Duraprep Surgical Solution is the first listed.
NCT01097135 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT01097135 about?
NCT01097135 is a clinical study titled "Evaluating the Effectiveness of 2 Surgical Skin Preparation Methods in Reducing Surgical Wound Drainage After Total Hip or Knee Replacement". Surgical skin complications can be costly and could contribute to extended in-patient stay following total joint replacement or even the need for re-admission. If efficacy in reducing the incidence of post-operative wound drainage and, in turn, surgical wound complications can be demonstrated, it ma...
What is the current status of trial NCT01097135?
This trial is currently completed. It is a NA study. The enrollment target is 600 participants. The study started on 2010-03. Estimated completion is 2012-12.
What conditions does trial NCT01097135 study?
This clinical trial studies the following conditions: Drainage.
What interventions are being tested in trial NCT01097135?
The interventions under investigation include: Duraprep Surgical Solution (DRUG).
Who is sponsoring clinical trial NCT01097135?
This trial is sponsored by Rothman Institute Orthopaedics, which has 23 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01097135 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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