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Effect of Preoperative Tramadol and Naproxen Sodium on Post Operative Pain

NCT05982392 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 47

Last updated 2024-08-07

No results posted yet for this study

Summary

The goal of this clinical trial is to compare in Tramadol, Naproxen sodium and Placebo in participants presenting with irreversible pulpitis in their mandibular posterior teeth.

The main question\[s\] it aims to answer are:

* Local anesthetic efficacy and .
* Postoperative pain. Participants will receive premedication treatments 60 minutes prior to the local anesthesia administration.

Researchers will compare Tramadol, Naproxen sodium and Placebo to evaluate their effects on Inferior alveolar nerve block efficacy and Postoperative pain.

Conditions

  • Symptomatic Irreversible Pulpitis
  • Post Operative Pain

Interventions

DRUG

Tramadol

Tramadol 100mg will be given 60 minutes before start of procedure.

DRUG

Naproxen Sodium

Naproxen sodium 550mg will be given 60 minutes before start of procedure.

DRUG

Placebo

Placebo will be given 60 minutes before start of procedure.

Sponsors & Collaborators

  • Dow University of Health Sciences

    lead OTHER

Principal Investigators

  • Tayyaba Tahira, BDS FCPS · Dow International Dental College, Dow University of Health Sciences

  • Farah Naz, BDS FCPS · Dow International Dental College, Dow University of Health Sciences

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-03-01
Primary Completion
2023-08-15
Completion
2023-08-15

Countries

  • Pakistan

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05982392 on ClinicalTrials.gov