Intraosseous vs Submucosal Injection of Dexamethasone

Status Completed

Clinical Trial Summary

Thirty-eight patients were randomly divided into 2 groups; the intraosseous injection group of dexamethasone (4 mg) and the submucosal injection group. All surgeries were performed by one surgeon. Postoperative pain was evaluated by visual analog scale score immediately after surgery and on postoperative days 1, 3, and 7. Swelling (determined using two linear measurements) were assessed just before the surgery and on postoperative days 1, 3, and 7 by using a digital vernier caliper. Early healing of periodontal soft tissue wound was assessed by using Early Wound Healing Score (EHS) which composed of 3 parameters: clinical signs of re-epithelization (CSR), clinical signs of hemostasis (CSH), and clinical signs of inflammation (CSI) and were assessed on postoperative days 1, 7, and 14. Mouth opening (determined by measurement of the maximum inter-incisal distance) were assessed just before the surgery and on postoperative days 1, 3, and 7 by using a digital vernier caliper.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Tooth, Impacted

Clinical Trial Details

NCT number	NCT04718077
Study type	Interventional
Source	Alexandria University
Contact
Status	Completed
Phase	N/A
Start date	August 1, 2020
Completion date	December 30, 2020

View Details

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