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NCT01050673 · ClinicalTrials.gov registry record · NA
Trial of Versajet Compared With Conventional Treatment in Acute and Chronic Wounds
A NA study of Surgical Wound Dehiscence, sponsored by Smith & Nephew.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
- 1
- Study location
NCT01050673: Completed NA study of Surgical Wound Dehiscence, sponsored by Smith & Nephew.
NCT01050673 is a NA study of Surgical Wound Dehiscence that has completed, run by Smith & Nephew. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01050673, a NA study of Surgical Wound Dehiscence, has completed, sponsored by Smith & Nephew.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
- 1
- Study location
Study Summary
It is increasingly recognised that the debridement of devitalised, bacterially contaminated or senescent tissue is an essential component of the effective treatment of delayed healing wounds. Whilst surgical debridement procedures have conventionally been performed with scalpels and other sharp instrumentation, alternative techniques such as the VERSAJET Hydrosurgery System are becoming more widespread. To increase the adoption of this new technology, it is essential that clinical improvements are assessed alongside the potential impact on the costs of debridement and the net financial impact on the hospital. It is hypothesised that a decrease in the time to achieve stable wound closure will not only lead to a patient benefit, but also a potential reduction in the cost of treatment due to e.g. repeat procedures, longer hospital stay, infection etc. The purpose of this study is to investigate the difference in time to closure of wounds surgically excised with VERSAJET Hydrosurgery System and those surgically excised using conventional operating room techniques.
Conditions Studied
Interventions
- DEVICE VERSAJET
- PROCEDURE Scalpel or blade
Study Locations (1)
Illinois
- Northwestern University Feinberg School of Medicine - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2007-11 |
| Est. Completion | 2011-09 |
| Phase | NA |
What the finished NCT01050673 record still lists
NCT01050673 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 1 condition, with Surgical Wound Dehiscence appearing as the primary indexed condition, and to 2 interventions - of which VERSAJET is the first listed.
NCT01050673 reports a single indexed study location in Illinois.
Frequently Asked Questions
What is clinical trial NCT01050673 about?
NCT01050673 is a clinical study titled "Trial of Versajet Compared With Conventional Treatment in Acute and Chronic Wounds". It is increasingly recognised that the debridement of devitalised, bacterially contaminated or senescent tissue is an essential component of the effective treatment of delayed healing wounds. Whilst surgical debridement procedures have conventionally been performed with scalpels and other sharp ins...
What is the current status of trial NCT01050673?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2007-11. Estimated completion is 2011-09.
What conditions does trial NCT01050673 study?
This clinical trial studies the following conditions: Surgical Wound Dehiscence.
What interventions are being tested in trial NCT01050673?
The interventions under investigation include: VERSAJET (DEVICE), Scalpel or blade (PROCEDURE).
Who is sponsoring clinical trial NCT01050673?
This trial is sponsored by Smith & Nephew, which has 72 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01050673 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT01050673's enrollment target sits among peer trials
40 1447th of 2000 higher than 465 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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