Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07400471

The Effects of Preemptive Multimodal Analgesic on Endodontic Pain Following Root Canal Therapy.

The Effects of Preemptive Multimodal Analgesic on Endodontic Pain.

Status
Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
280 (estimated)
Sponsor
Chattogram International Dental College · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

A clinical trial comparing preemptive multimodal analgesics with placebo in the management of immediate and chronic post-endodontic pain. The study utilizes statistical methods such as chi-squared, T-tests, and regression analysis, accounting for multiple outcomes with the Bonferroni adjustment. Duloxetine hydrochloride and pregabalin, both available in Bangladesh, are evaluated as experimental drugs, while placebos are used to assess psychological effects on pain. All participants receive standard interventional treatments, with acetaminophen provided as needed, and ethical considerations are addressed according to international guidelines.

Conditions

Interventions

TypeNameDescription
DRUGPregabalin- AcetaminophenPreemptive Multi modal analgesic drug: Experimental group will be divided into 2 subgroups according to use of drug. A. Pregabalin-acetaminophen. B. Duloxetine-Acetaminophen Pregabalin-acetaminophen: Before a half-hour endodontic treatment, patients in this group will receive a single dosage of 50 mg pregabalin and 500 mg acetaminophen. If necessary, acetaminophen dosages of 500 mg will be administered three times a day.
DRUGDuloxetine- AcetaminophenDuloxetine-Acetaminophen: Prior to a half-hour endodontic treatment, patients in this group will receive a single dosage of 500 mg of acetaminophen and 30 mg of Duloxetine. If necessary, acetaminophen dosages of 500 mg will be administered three times a day.

Timeline

Start date
2026-02-06
Primary completion
2027-03-30
Completion
2027-04-30
First posted
2026-02-10
Last updated
2026-02-11

Locations

1 site across 1 country: Bangladesh

Source: ClinicalTrials.gov record NCT07400471. Inclusion in this directory is not an endorsement.