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NCT00855569 · ClinicalTrials.gov registry record

Hemostatic Textile to Control Bleeding at Donor Graft Sites

A clinical trial, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
20
Enrollment target

NCT00855569: Completed study, sponsored by University of North Carolina, Chapel Hill.

NCT00855569 is a clinical trial that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 20 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00855569 has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
20 participants
Enrollment target

Study Summary

The rationale underlying the study is that donor site bleeding is common and often problematic when presenting to the burn surgeon or staff. Frequently, gauze wound dressings are not sufficiently hemostatic to control a donor site bleed thereby leading to administration of vasoconstrictive agents and repeated application of wound dressing/pressure. The hemostatic textile Stasilon™ has proven superior to gauze in reducing bleeding from anesthetized pigs undergoing standardized surgically-induced trauma. Also, observational case reports have noted cessation of bleeding in a limited number of human patients with difficult to control bleeds.

Interventions

  • DEVICE Stasilon

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2008-06
Est. Completion 2010-12

What the finished NCT00855569 record still lists

NCT00855569 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Stasilon is the first listed.

NCT00855569 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00855569 about?

NCT00855569 is a clinical study titled "Hemostatic Textile to Control Bleeding at Donor Graft Sites". The rationale underlying the study is that donor site bleeding is common and often problematic when presenting to the burn surgeon or staff. Frequently, gauze wound dressings are not sufficiently hemostatic to control a donor site bleed thereby leading to administration of vasoconstrictive agents an...

What is the current status of trial NCT00855569?

This trial is currently completed. The enrollment target is 20 participants. The study started on 2008-06. Estimated completion is 2010-12.

What interventions are being tested in trial NCT00855569?

The interventions under investigation include: Stasilon (DEVICE).

Who is sponsoring clinical trial NCT00855569?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00855569, the US trial registry maintained by the National Library of Medicine. NCT00855569 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.