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NCT02799667 · ClinicalTrials.gov registry record · NA
Do Single Use Negative Pressure Dressings Reduce Wound Complications in Obese Women After Cesarean Delivery
A NA study, sponsored by Tufts Medical Center.
- Terminated
- Registry status
- NA
- Development phase
- 110
- Enrollment target
NCT02799667: Clinical Trial NA study, sponsored by Tufts Medical Center.
NCT02799667 is a NA study that was terminated before completion, run by Tufts Medical Center. The registered enrollment target is 110 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02799667, a NA study, was terminated before completion, sponsored by Tufts Medical Center.
- TERMINATED
- Registry status
- NA
- Development phase
- 110 participants
- Enrollment target
Study Summary
The investigators aim to show that single use negative pressure dressings can decrease the rate of wound complications in obese women (BMI \> 40 kg/m2) undergoing cesarean delivery at a tertiary medical center by randomizing women to receive either a single use negative pressure dressing or the standard dressing after cesarean delivery.
Primary Outcome
Composite outcome of wound complications, defined as the presence of any of the following: superficial, deep, and organ space surgical site infections (SSIs), skin blisters around the incision, scar separation \>1 cm, seroma requiring evacuation, hematoma requiring evacuation, wound debridement, hospital re-admission, and additional operating room management.
Interventions
- DEVICE Standard Dressing
- DEVICE Negative Pressure Wound Therapy Dressing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 110 participants |
| Start Date | 2016-05 |
| Est. Completion | 2019-03-31 |
| Phase | NA |
Why NCT02799667 stopped before completion
NCT02799667 is an interventional study that assigns participants to a tested intervention. The registered 110 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 (92% lower).
The record links to 0 conditions, and to 2 interventions - of which Standard Dressing is the first listed.
NCT02799667 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02799667 about?
NCT02799667 is a clinical study titled "Do Single Use Negative Pressure Dressings Reduce Wound Complications in Obese Women After Cesarean Delivery". The investigators aim to show that single use negative pressure dressings can decrease the rate of wound complications in obese women (BMI \> 40 kg/m2) undergoing cesarean delivery at a tertiary medical center by randomizing women to receive either a single use negative pressure dressing or the stan...
What is the current status of trial NCT02799667?
This trial is currently terminated. It is a NA study. The enrollment target is 110 participants. The study started on 2016-05. Estimated completion is 2019-03-31.
What interventions are being tested in trial NCT02799667?
The interventions under investigation include: Standard Dressing (DEVICE), Negative Pressure Wound Therapy Dressing (DEVICE).
Who is sponsoring clinical trial NCT02799667?
This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02799667's enrollment target sits among peer trials
110 816th of 2000 higher than 1,176 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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