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NCT01637870 · ClinicalTrials.gov registry record · NA
Negative Pressure Wound Therapy After Cesarean Delivery
A NA study, sponsored by Abbey Hardy-Fairbanks.
- Completed
- Registry status
- NA
- Development phase
- 110
- Enrollment target
NCT01637870 is a NA study that has completed, run by Abbey Hardy-Fairbanks. The registered enrollment target is 110 participants.
The verdict
NCT01637870, a NA study, has completed, sponsored by Abbey Hardy-Fairbanks.
- COMPLETED
- Registry status
- NA
- Development phase
- 110 participants
- Enrollment target
Study Summary
This study is aimed at determining whether or not the use of a wound suction device placed on the cesarean incision instead of a standard sterile dressing will decrease the prevalence of wound complications and wound infections in women at high risk for post operative complications. The study will first look at the infection and wound complication rate in women 6 months prior to the start date of the study by reviewing charts of women who have undergone a cesarean section. The study involves placing a single use, portable wound vacuum over the cesarean section incision and keeping it in place for 72h. The investigators will then compare the rates of wound infection and wound complications between these two groups. It is our hypothesis that negative pressure wound systems will decrease the wound infection and complication rate in this high risk population.
Interventions
- DEVICE Prevena negative pressure wound system
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2012-08 |
| Est. Completion | 2013-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01637870
The ClinicalTrials.gov registry entry for NCT01637870 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 110 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbey Hardy-Fairbanks, which has 2 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Prevena negative pressure wound system is the first listed.
NCT01637870 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01637870 about?
NCT01637870 is a clinical study titled "Negative Pressure Wound Therapy After Cesarean Delivery". This study is aimed at determining whether or not the use of a wound suction device placed on the cesarean incision instead of a standard sterile dressing will decrease the prevalence of wound complications and wound infections in women at high risk for post operative complications. The study will f...
What is the current status of trial NCT01637870?
This trial is currently completed. It is a NA study. The enrollment target is 110 participants. The study started on 2012-08. Estimated completion is 2013-02.
What interventions are being tested in trial NCT01637870?
The interventions under investigation include: Prevena negative pressure wound system (DEVICE).
Who is sponsoring clinical trial NCT01637870?
This trial is sponsored by Abbey Hardy-Fairbanks, which has 2 total clinical trials registered on ClinicalTrials.gov.
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