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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00392301
Other study ID # 2006-0094
Secondary ID
Status Withdrawn
Phase N/A
First received October 23, 2006
Last updated February 20, 2018
Start date October 2009
Est. completion date July 1, 2012

Study information

Verified date February 2018
Source University of Mississippi Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this research study is to discover whether instruments widely used in skin research can be used to measure wound healing in split thickness skin graft donor sites and whether these instruments can detect differences in healing when two different dressing products are used.


Description:

Currently there is no standard treatment to promote wound healing for split thickness skin graft donor sites and healing is determined based on clinical observation of the graft donor site and clinical judgement. Here we propose to use two instruments commonly used in skin research to measure wound healing. This study will validate the use of these two instruments, one that measures transepidermal water loss and the other that measures skin pigmentation to determine healing. To further validate the use of these instruments we will determine if these instruments can detect differences between two different wound dressing products that have been previously reported to heal skin graft donor sites at different rates.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 1, 2012
Est. primary completion date July 1, 2012
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Participants 18 years of age and over who have a split-thickness skin graft donor site.

Exclusion Criteria:

- Individuals under 18 years of age.

- Individuals who do not have a split thickness skin graft donor site.

Study Design


Related Conditions & MeSH terms

  • Split-thickness Skin Graft Donor Sites

Locations

Country Name City State
United States University of Mississippi Medical Center Jackson Mississippi

Sponsors (1)

Lead Sponsor Collaborator
University of Mississippi Medical Center

Country where clinical trial is conducted

United States, 

References & Publications (6)

Disa JJ, Alizadeh K, Smith JW, Hu Q, Cordeiro PG. Evaluation of a combined calcium sodium alginate and bio-occlusive membrane dressing in the management of split-thickness skin graft donor sites. Ann Plast Surg. 2001 Apr;46(4):405-8. — View Citation

Feldman DL, Rogers A, Karpinski RH. A prospective trial comparing Biobrane, Duoderm and xeroform for skin graft donor sites. Surg Gynecol Obstet. 1991 Jul;173(1):1-5. — View Citation

Feldman DL. Which dressing for split-thickness skin graft donor sites? Ann Plast Surg. 1991 Sep;27(3):288-91. Review. — View Citation

Kilinç H, Sensöz O, Ozdemir R, Unlü RE, Baran C. Which dressing for split-thickness skin graft donor sites? Ann Plast Surg. 2001 Apr;46(4):409-14. — View Citation

Malpass KG, Snelling CF, Tron V. Comparison of donor-site healing under Xeroform and Jelonet dressings: unexpected findings. Plast Reconstr Surg. 2003 Aug;112(2):430-9. — View Citation

Rakel BA, Bermel MA, Abbott LI, Baumler SK, Burger MR, Dawson CJ, Heinle JA, Ocheltree IM. Split-thickness skin graft donor site care: a quantitative synthesis of the research. Appl Nurs Res. 1998 Nov;11(4):174-82. Review. — View Citation

See also
  Status Clinical Trial Phase
Completed NCT01512017 - Clinical Study on Veloderm for the Treatment of Split-thickness Skin Graft Donor Sites Phase 3
Withdrawn NCT02712164 - Molecular, Histologic, and Clinical Analysis of Negative Pressure Wound Therapy (NPWT) for Split-thickness Skin Graft (STSG) Donor Sites N/A
Completed NCT02642679 - Evaluation of Opticell Ag on Split-Thickness Skin Graft Donor Sites in Adult Subjects N/A