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臨床試驗

Use of Silk Fibroin Dressings in Primary Total Hip Arthroplasty

NCT:NCT07868900 · NOT_YET_RECRUITING

NCT IDNCT07868900
狀態NOT_YET_RECRUITING
開始日期2026-10-15
完成時間2028-01-01
SponsorThe University of Texas Health Science Center, Houston (OTHER)
First posted
Last updated

簡要摘要

The purpose of this study is to document the incidence of allergic contact dermatitis (ACD) to silk fibroin and 2-octyl cyanoacrylate mesh dressings, to document the incidence of acute wound dehiscence requiring reoperation after application of silk fibroin and 2-octyl cyanoacrylate mesh dressings, to identify differences in clinic utilization for complications related to silk fibroin and 2-octyl cyanoacrylate mesh dressings and to collect patient reported outcome measures (PROMs) related to patient comfort and satisfaction for silk fibroin and 2-octyl cyanoacrylate mesh dressings after total hip arthroplasty.

官方來源

在 ClinicalTrials.gov 上查看 →

資料來自 ClinicalTrials.gov API。最新狀態請參閱官方紀錄。

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