Actively Recruiting

Early Phase 1
Age: 18Years +
All Genders
Healthy Volunteers
NCT07400471

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

Led by Chattogram International Dental College · Updated on 2026-02-11

280

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older
  • ASA physical status I or II
  • Patients with pain originating from teeth and surrounding areas
  • Preoperative pain severity is moderate to severe
  • Patients able to communicate about their pain
  • Patients who give consent to participate in the study
  • Patients with other chronic pain conditions
  • Patients scheduled for non-surgical endodontic treatment
  • Patients scheduled for non-surgical endodontic retreatment
  • Patients scheduled for surgical endodontic treatment
Not Eligible

You will not qualify if you...

  • Patients who do not wish to participate in the study
  • Patients with medical conditions contraindicating study drugs
  • ASA physical status III, IV, or V
  • Patients currently treated with anti-convulsant drugs
  • Patients participating in other clinical trials
  • Patients with poor motivation or adherence to study protocols
  • Pregnant patients
  • Patients with severe organ dysfunction
  • Patients with hepatitis B or other infectious diseases like HIV
  • Patients with uncontrolled comorbidities unsuitable for endodontic treatment
  • Patients with severe cognitive impairment
  • Patients with history of certain cancers or severe blood disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Professor. Dr. Md. Abu Saeed Ibn Harun

Chittagong, Chattogram, Bangladesh, 4212

Actively Recruiting

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Research Team

P

Prof.Dr. Md. Abu Saeed Ibn Harun, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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