TerminatedNot Applicable

The Effect of Platelet Rich Plasma on Pain at Skin Graft Donor Sites

Stopped: Suspended per IRB

United States25 participantsStarted 2019-11-01

Plain-language summary

The purpose of this study is to compare post-operative skin graft donor site pain between those treated with standard wound care vs PRP. Secondarily the study is designed to compare time to complete donor site healing. The null hypothesis is that here is no difference in post-operative donor site pain between those treated with standard wound care and PRP. The secondary null hypothesis is that there is no difference in time to donor site healing.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Any patient requiring a split thickness skin graft and is above the age of 18. Exclusion Criteria: * Medical history of chronic pain at the donor site * Inability to follow up * Unable to participate in pre or post operative questionnaire inclusive of organic * Traumatic, chemical or degenerative causes of altered mental sensorium * Age \<18.

What they're measuring

Patient post-operative donor site pain.

Timeframe: Through study completion, an average of 1 year

Duration of donor site wound

Timeframe: Through study completion, an average of 1 year

Opioid consumption

Timeframe: Through study completion, an average of 1 year

Trial details

NCT IDNCT03937765

SponsorUniversity of Arizona

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-03-15

View on ClinicalTrials.gov More Skin Graft (Allograft) Rejection trials