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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01750034
Other study ID # 12-2288
Secondary ID
Status Withdrawn
Phase N/A
First received December 12, 2012
Last updated September 2, 2015
Start date June 2015
Est. completion date July 2016

Study information

Verified date September 2015
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to better understand how to best care for burn wounds.


Description:

Participants: Patients presenting to Kamuzu Central Hospital in Lilongwe Malawi with burn wounds occuring within 72 hours of admission.

Procedures (methods): This is a prospective randomized trial. Subjects will be randomized during admission to receive either open dressing care or closed dressing care of their burn wounds.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 2016
Est. primary completion date June 2016
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Burn wound admitted to the hospital

- Signed informed consent

- Burn wound occuring within 72 hours of admission

Exclusion Criteria:

- Language other than Chichewa or English

- Inability to access of phone (required for follow-up)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Closed method
Subjects will have their wounds managed by covering with gauze and changing this gauze 3 to 7 times per week.
Open method
Subjects will have their burns managed by keeping the wounds exposed to the air.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill

References & Publications (5)

Dominguez O, Bains JW, Lynch JB, Lewis SR. Treatment of burns with silver nitrate versus exposure method: analysis of 200 patients. Plast Reconstr Surg. 1967 Nov;40(5):489-93. — View Citation

Gosselin RA, Kuppers B. Open versus closed management of burn wounds in a low-income developing country. Burns. 2008 Aug;34(5):644-7. doi: 10.1016/j.burns.2007.09.013. Epub 2008 Jan 15. — View Citation

HOLMAN SP, SHAYA ES, HOFFMEISTER FS, EDGERTON MT Jr. Studies on burns. I. The exposure method vs. occlusive dressings in the local treatment of experimental burns. Ann Surg. 1956 Jan;143(1):49-56. — View Citation

Kiser MM, Samuel JC, Mclean SE, Muyco AP, Cairns BA, Charles AG. Epidemiology of pediatric injury in Malawi: burden of disease and implications for prevention. Int J Surg. 2012;10(10):611-7. doi: 10.1016/j.ijsu.2012.10.004. Epub 2012 Nov 7. — View Citation

Samuel JC, Campbell EL, Mjuweni S, Muyco AP, Cairns BA, Charles AG. The epidemiology, management, outcomes and areas for improvement of burn care in central Malawi: an observational study. J Int Med Res. 2011;39(3):873-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Microbiologic profile of clinical infections Qualitative microbiologic culture results and sensitivity panels from surface swabs taken from infected burn wounds (as defined by clinical criteria described in the secondary outcome "burn wound infection rate"). 30-day Yes
Other Number of surgical procedures Number of surgical procedures required including indication and type of procedure. 30-day Yes
Other percent skin graft survival Percent survival (defined as area surviving / total area grafted at 7 days) of skin grafts. 30-day Yes
Other Hospital length of stay Length of stay during initial hospitalization. 30-day Yes
Primary Time to healing Time from burn injury to healing (defined as at least 90% epithelialization) as determined by hospital records, outpatient clinical records and telephone contact (with subject or next-of-kin) per study protocol. 30-day Yes
Secondary Mortality Mortality within 30 days of burn injury, as determined by hospital records, outpatient clinical records and telephone contact (with next-of-kin) per study protocol. 30-day Yes
Secondary Burn wound infection rate Clinical suspicion of infection defined by presence of (a) burn wound cellulitis (erythema and/or edema AND pain and/or tenderness at the border of the wound), or (b) burn wound infection (change in appearance of the burn including focal or multifocal brown, black or violaceous discoloration OR rapid separation of the eschar OR conversion of partial thickness to full thickness burn). 30-day Yes
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