Range of Motion Following Intraoperative Coban Dressing Application in Hand Burns

Burns Clinical Trial

Official title:

Day One Post Operative Range of Motion Following Skin Graft to Hand With Intraoperative Coban Dressing

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01027520
• Other study ID #: cobandressing
• Status: Terminated
• Phase: N/A
• First received: December 4, 2009
• Last updated: September 6, 2017
• Start date: January 2010
• Est. completion date: December 2011

Study information

• Verified date: September 2016
• Source: University of Missouri-Columbia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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?

Description:

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 6
• Est. completion date: December 2011
• Est. primary completion date: December 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Burns
• Hand Injuries

Intervention

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

Locations

Country	Name	City	State
United States	University of Missouri Health Care - George David Peak Memorial Burn Center	Columbia	Missouri

Sponsors (1)

Lead Sponsor	Collaborator
University of Missouri-Columbia

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	hand function(range of motion, grip and pinch strength)		post operative day four, first, second and third clinic visits
Secondary	graft success		post operative day 4 and first, second and third clinic visits