Range of Motion Following Intraoperative Coban Dressing Application in Hand Burns

Official Title: “Day One Post Operative Range of Motion Following Skin Graft to Hand With Intraoperative Coban Dressing”

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?

The participant will be evaluated by occupational therapist prior to surgery. The coban dressing will be applied to the participant's hand(s)during surgery for a skin graft. This portion will occur whether the participant agrees to participate or not. The participant will begin range of motion exercises the day after surgery (post operative day one) with and occupational therapist. The occupational therapist will see the participant daily for supervised range of motion while in the hospital. The coban dressing will be removed on post operative day one if a sheet graft is placed to assess bleeding under graft. The coban dressing will be reapplied and removed again on post operative day four. When a meshed graft is placed, coban dressing will be removed on post operative day four only. All skin grafts (meshed and sheet grafts) and range of motion will be assessed on post operative day four. Coban dressing will be reapplied. The participant will continue range of motion exercise program at home. An appointment will be scheduled for 3 consecutive weeks in out patient burn clinic. During clinic visits, skin graft, range of motion, and grip strength will be measured. The participant will seen in out patient burn clinic whether they choose to participate in the study or not as a standard of burn care.

Intervention(s) in this Clinical Trial

• Other: application of coban dressing
  • application of a intraoperative coban dressing with reapplications following dressing removal.

Primary Measures

• hand function(range of motion, grip and pinch strength)
  • Time Frame: post operative day four, first, second and third clinic visits
    Safety Issue?: No

Secondary Measures

• graft success
  • Time Frame: post opeartive day 4 and first, second and third clinic visits
    Safety Issue?: Yes

Inclusion Criteria:

• Less than 15% burn, burn requires skin graft to dorsum of hand, burn involves at least 2 metacarpophalangeal joints
• 18 and older

Exclusion Criteria:

• Latex allergy
• Documented diagnoses of mental illness that interferes with patients ability to participate

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers

Lead Investigator: University of Missouri-Columbia Other

Overall Clinical Trial Officials and Contacts

Overall Contact: Catherine Lynn Barrow, BS OT 573-882-8706 barrowc@health.missouri.edu

Information obtained from ClinicalTrials.gov on February 09, 2012

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT01027520

Study ID Number: cobandressing

ClinicalTrials.gov Identifier: NCT01027520

Health Authority: University of Missouri, USA: Health Science Institutional Review Board