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Clinical Trial Summary

CTG was harvested from 21 patients in each group. Donor site was treated with either GS (control) or GS+CY (test). Palatal tissue thickness, graft dimensions, working time (WT) and primary bleeding time were recorded intraoperatively. Patients recorded the quantity of analgesics (QA) taken, presence of secondary bleeding (SB) and pain perception (PP) daily for first postoperative week. Sensation loss (SL), color match (CM), epithelization level (EL) were evaluated at days 7, 14, 21 and 28.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04403503
Study type Interventional
Source Hacettepe University
Contact
Status Completed
Phase N/A
Start date July 1, 2018
Completion date March 1, 2019

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