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Comparison of Pre-Operative Versus Post-Operative Dexamethasone Administration on Post-Operative Complications in Lower Third Molar Surgery using Saline as a Control: A Randomized Clinical Trial with

Comparative Analysis of Pre- and Postoperative Dexamethasone Administration in Lower Third Molar Surgery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2025/001
Enrollment
Unknown
Registered
2025-01-21
Start date
2025-01-22
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bony impacted lower third molars.

Interventions

The study will be conducted in a clinical-based setting, specifically within the Department of Oral Surgery at Oman Dental College, located in Muscat, Oman. Patients planned for lower third molar su

Sponsors

Oman Dental College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion Criteria: - * All ages * Both men and women * Individuals officially diagnosed with lower bony impacted third molars. Diagonosis is according to winter’s classification (horizontal, vertical, mesioangular, distoangular). OPGs (orthopantomogram) will be taken for all participants. Using this radiograph, the type of impaction will be determined. * Patients scheduled to undergo surgical extraction of bony impacted lower third molar surgery at the oral Surgery Department in Oman Dental College. • Patients must possess the ability to self-administer the questionnaire. This includes having the literacy and comprehension skills necessary to understand and respond accurately to the modified validated Arabic version of the Post-operative symptoms following surgical removal of lower wisdom teeth Questionnaire.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: • Patients who took pre-op antibiotics. • Individuals with cognitive impairments that impede their ability to understand the consent process or to accurately fill out the questionnaires. • Patients with None bony impaction that might affect the surgery's outcomes or their ability to participate fully in the study.

Design outcomes

Primary

MeasureTime frame
1.Visual analogue scale: a modified validated Arabic version, consisting of 15 questions across 3 sections: pain, swelling and trismus. The score ranges from 0 to 5, with lower scores indicating better outcomes. [[post surgery for 5 days on each day]]

Secondary

MeasureTime frame
None [None]

Countries

Oman

Contacts

Public ContactAmur Alsenaidi

Assistant Professor

aalsenaidi@staff.odc.edu.om96894388846

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Sep 19, 2026