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Dexamethasone Treatment for Patients Undergoing Endodontics

Sponsored by University of Salamanca

About this trial

Last updated a year ago

Study ID

U1111-1320-4208

Status

Completed

Type

Interventional

Phase

Phase 4

Placebo

No

Accepting

20 to 50 Years
All Sexes

Trial Timing

Ended a year ago

What is this trial about?

This Phase IV randomized clinical trial (RCT) evaluated the efficacy of preoperative administration of a single 4 mg oral dose of dexamethasone in reducing postoperative pain and inflammation following endodontic treatment. Conducted at the Department of Endodontics, PhD Program, Faculty of Dentistry, University of Salamanca, the study included 82 participants who were randomly assigned to either the test group (preoperative dexamethasone) or the control group (postoperative ibuprofen 400 mg every 4 hours). Pain intensity was measured using the Visual Analog Scale (VAS) at 4, 6, 8, 12, and 24 hours postoperatively. Results indicated significantly lower pain perception in the dexamethasone group compared to the ibuprofen group at all time points, with the majority of dexamethasone-treated patients reporting only mild pain. No adverse effects were observed in either group, and no patient required additional rescue analgesia. The findings suggest that a single preoperative dose of dexamethasone is a safe and effective strategy for managing postoperative pain in endodontic procedures, providing superior analgesia compared to the standard postoperative ibuprofen regimen. Keywords: Endodontic pain, dexamethasone, preoperative analgesia, randomized clinical trial, inflammation control, corticosteroids, endodontics.

What are the participation requirements?

Inclusion Criteria

* Participants must meet all of the following criteria to be eligible for the study: * Age Range: 20 to 50 years old. * Indication for Endodontic Treatment: Patients requiring root canal therapy due to irreversible pulpitis (with or without apical lesion), pulp necrosis, retreatment with periapical lesion, or endodontic surgery. * Eligible Teeth: Any dental group (anterior, premolar, molar, both maxillary and mandibular). * General Health Status: Classified as ASA I (healthy individuals without systemic conditions) according to the American Society of Anesthesiologists (ASA) Physical Status Classification. * Consent: Willingness to participate in the study and ability to provide signed informed consent.

Exclusion Criteria

* Participants will be excluded if any of the following conditions apply: * Age: Under 20 or over 50 years old. * Medical Conditions: Immunocompromised individuals (e.g., HIV/AIDS, cancer patients undergoing chemotherapy). Systemic diseases such as diabetes mellitus, osteoporosis, acute psychosis, glaucoma, cataracts. Patients with tuberculosis or systemic fungal infections. Gastrointestinal conditions such as ulcerative colitis, peptic ulcers, or diverticulitis. -Medication Use: Use of NSAIDs or corticosteroids within 48 hours prior to the intervention. Regular use of barbiturates. -Dental Factors: Tooth fractures involving the roots. Severe dental hypersensitivity that may interfere with pain assessment. -Pregnancy and Lactation: Pregnant or breastfeeding women will be excluded due to potential effects of dexamethasone. -Non-Compliance: Patients who decline participation or are unwilling to follow study procedures, including pain assessment and follow-up.