Range of Motion Following Intraoperative Coban Dressing Application in Hand Burns
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|ClinicalTrials.gov Identifier: NCT01027520|
Recruitment Status : Terminated (Insufficient enrollment numbers)
First Posted : December 8, 2009
Last Update Posted : September 11, 2017
Participants of this study will include burns requiring skin graft to hand(s). After informed consent, an occupational therapy evaluation will be performed. Participants will consent to surgery, in which skin graft will be applied by physician during surgery, occupational therapy will apply coban dressing. Participant will seen daily by occupational therapist during hospitalization for active range of motion to hand(s). Occupational therapist will measure range of motion of hand(s) and physician will assess graft success at one and four days after surgery and at three out patient clinic visits. Hand strength will also be measured at three out patient visits.
Does the initiation of range of motion on post operative day kone with coban dressing improve hand function without compromising graft success?
|Condition or disease||Intervention/treatment|
|Burns Hand Injuries||Other: application of coban dressing|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||6 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Day One Post Operative Range of Motion Following Skin Graft to Hand With Intraoperative Coban Dressing|
|Study Start Date :||January 2010|
|Primary Completion Date :||December 2011|
|Study Completion Date :||December 2011|
Application of Coban dressing
Other: application of coban dressing
application of a intraoperative coban dressing with reapplications following dressing removal.
Other Name: 3M Coban Self-Adherent wrap
- hand function(range of motion, grip and pinch strength) [ Time Frame: post operative day four, first, second and third clinic visits ]
- graft success [ Time Frame: post operative day 4 and first, second and third clinic visits ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01027520
|United States, Missouri|
|University of Missouri Health Care - George David Peak Memorial Burn Center|
|Columbia, Missouri, United States, 65212|
|Principal Investigator:||Catherine L Barrow, BS OT||University of Missouri-Columbia|