Clinical Trials Directory

Trials / Completed

CompletedNCT04718077

Intraosseous vs Submucosal Injection of Dexamethasone

Effectiveness of Intraosseous Injection of Dexamethasone Following Impacted Mandibular Third Molar Removal (Randomized Controlled Clinical Trial)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Hams Hamed Abdelrahman · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERIntraosseusIO dexamethasone injection Dexamethasone 4 mg
OTHERSubmucoalSM dexamethasone injection Dexamethasone 4 mg

Timeline

Start date
2020-08-01
Primary completion
2020-12-30
Completion
2020-12-30
First posted
2021-01-22
Last updated
2021-01-22

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04718077. Inclusion in this directory is not an endorsement.