Skip to main content
OpenTrials
Active, Not Recruiting

NCT Number: NCT07538375

Effectiveness of Dexamethasone Injection for Reducing Pain After Third Molar Surgery

This randomized clinical trial aims to evaluate the effectiveness of dexamethasone injection in reducing postoperative pain after surgical removal of impacted mandibular third molars. Patients are divided into two groups: one receiving standard local anesthesia, and the other receiving an additional dexamethasone injection postoperatively. Pain levels are assessed using the Visual Analogue Scale (VAS) at 24, 48, and 72 hours after surgery. The study is conducted at 28 Military Dental Centre, Lahore.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

20 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

28 Military Dental Centre

Lahore, Punjab Province, 63000, Pakistan

About this study

Impacted mandibular third molar surgery is commonly associated with postoperative pain, which can affect patient comfort and recovery. Corticosteroids such as dexamethasone have anti-inflammatory properties and may reduce postoperative pain and swelling.

This randomized clinical trial is designed to compare postoperative pain levels in patients undergoing third molar surgery with and without the administration of dexamethasone. Patients are randomly allocated into two groups. Group 1 receives standard inferior alveolar nerve block using 2% lignocaine with epinephrine. Group 2 receives an additional 1 ml (8 mg) dexamethasone injection in the buccal vestibule after completion of surgery.

Pain is assessed using the Visual Analogue Scale (VAS) at 24, 48, and 72 hours postoperatively. All patients are prescribed the same postoperative analgesic regimen. The primary outcome is the difference in mean pain scores between the two groups. Data analysis is performed using SPSS, and statistical significance is set at p < 0.05.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 20 to 40 years
  • Patients with at least one impacted mandibular third molar (Class A or B, Class I or II) including mesioangular, horizontal, vertical, or distoangular impactions according to Pell and Gregory classification confirmed by panoramic radiograph
  • Patients with no systemic disease (e.g., diabetes mellitus, hypertension, ischemic heart disease)
  • Patients of either gender

Exclusion criteria

  • Patients who have used analgesics or related drugs within 15 days prior to surgery
  • Pregnant patients
  • Patients with known allergy to corticosteroids
  • Patients with tooth associated with cyst, tumor, or trauma

Treatment and study plan

Dexamethasone

Drug

Dexamethasone 8 mg (1 ml) was administered via buccal vestibular injection immediately after surgical removal of impacted mandibular third molars.

Primary outcomes

  1. Postoperative pain intensity

    Time frame: 24 hours, 48 hours, and 72 hours postoperatively

    Postoperative pain will be assessed using a 10-point Visual Analog Scale (VAS), where 0 indicates no pain and 10 indicates worst possible pain, following surgical removal of impacted mandibular third molars.

Sponsors and collaborators

Lead sponsor

28 Military Dental Centre Lahore

Other Gov

Registry information

Official study title

Effectiveness of Dexamethasone Injection on Postoperative Pain After Impacted Third Molar Surgery Assessed Using Visual Analog Scale

Acronym: DEXA-TMS

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 20, 2026
Registry last updated
Apr 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.