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UT Health San Antonio

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Pilot Study to Compare Topical Voriconazole to Placebo as a Pain Reducing Agent

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Privacy Notice: The data collected here will be used by UT Health San Antonio staff to contact you, either by email or by telephone, with the sole purpose of providing you with information regarding human study participation. You may be contacted in the future regarding studies similar to this one. Under no circumstances will we use your information for other purposes or share it with others. To the extent it is applicable, UT Health San Antonio complies with the General Data Protection Regulation (“GDPR”). Should you have any requests pertaining to your rights under the GDPR, please send it to: The Office of Clinical Research ocrmail@uthscsa.edu | (210) 567-8555

Lay Description

This study seeks to test if the study drug (voriconazole), when applied topically to a burn wound on the skin will help to reduce pain.

Eligibility

Eligible Ages: Between 18 Years and 60 Years
Eligible Genders: All
Accepts Healthy Volunteers: No

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Exclusion Criteria

Study Design

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Yes, I would like to be contacted about studies in the same category or cancer site

Andrew Carrillo
(210) 567-0383
carrilloa3@uthscsa.edu

Lavanya Pandranki
(210) 562-4171
pandranki@uthscsa.edu

Andrew Carrillo
(210) 567-0383
carrilloa3@uthscsa.edu

Lavanya Pandranki
(210) 562-4171
pandranki@uthscsa.edu

Principal Investigator
Sunil Ahuja

UT Health San Antonio

8403 Floyd Curl Dr
San Antonio, TX 78229

210-567-8555
OCRMail@uthscsa.edu

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