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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: Completed NA study of Drainage, sponsored by Rothman Institute Orthopaedics.
NCT01097135 is a NA study of Drainage that has completed, run by Rothman Institute Orthopaedics. The registered enrollment target is 600 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Starting on post operative day 1 (the first day following surgery), at the time of the surgical dressings are removed and changed, assessments will be made to determine level of post-operative wound drainage following TJA.
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 |
What the finished NCT01097135 record still lists
NCT01097135 is an interventional study that assigns participants to a tested intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (57% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
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Where NCT01097135's enrollment target sits among peer trials
600 162nd of 2000 higher than 1,827 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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