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To Study Gene Expression of Postburn Hypertrophic Scar

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National Taiwan University

Status

Unknown

Conditions

Cicatrix, Hypertrophic

Study type

Observational

Funder types

Other

Identifiers

NCT01676168
201205098RIC

Details and patient eligibility

About

Aim: To compare the gene expression of postburn hypertrophic scar with normal skin.

Full description

Background: Postburn hypertrophic scar (HS) remains a challenging problem. Although varied clinical therapeutic methods have been used, none of them has been widely accepted as a standard care. As hypertrophic scar is hereditary, gene therapy can be a potential tool for scar treatment. To investigate the correlation between the clinical presentation of the hypertrophic scar and its gene expression, we propose an analysis of gene expression in the hypertrophic scar using DNA microarray and Real-Time Quantitative PCR. The study result may form the base of clinical treatment.

Methods and Materials: Thirty scar patients requiring surgical treatment in NTUH burn center will be enrolled into the study. Inclusion criteria: (1) Age between 20 and 80 (2) Patients with postburn hypertrophic scar require surgical treatment.

  1. Hypertrophic scar and normal skin collection: Under Clinical Trial Informed Consent of Research Ethic Committee, scar and normal skin specimen of 1x1cm2 each will be collected and transported to tissue bank with a vacuum low temperature container. The specimen will be kept in a -80℃ refrigerator.
  2. RNA extraction from skin tissue: The RNA extraction will be performed using kit available in the market. Spectrophotometer and gel electrophoresis will be used to measure the purity and concentration of RNA.
  3. Gene expression analysis: DNA microarray and Real-Time Quantitative PCR will be used to analyze RNA expression of hypertrophic scar and normal skin.

Statistics: Student's t-test will be used to compare statistically gene expression between hypertrophic scar and normal skin. P < 0.05 will be considered as statistical significance.

Enrollment

30 estimated patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age20~80, hypertrophic scar patient

Exclusion criteria

  • no specific limitation

Trial design

30 participants in 2 patient groups

hypertrophic scar
Description:
1x1cm2 hypertrophic scar of post-burn patients are taked by visiting staff when they accept scar-reconstructive surgery.
normal skin
Description:
When the patient accept skin grafting surgery, visiting staff will take 1x1cm2 normal skin.

Trial contacts and locations

1

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Central trial contact

Kean Eng Yeong, college

Data sourced from clinicaltrials.gov

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