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Pretreatment Aceclofenac Effect on Pain and Analgesic Intake After Endodontic Treatment

NCT03335007 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2017-11-07

No results posted yet for this study

Summary

The aim of this prospective, randomized, double-blind, clinical trial is to evaluate the effect of a preoperative, single, oral dose of aceclofenac (100 mg) on postendodontic pain at 6, 24 and 48 hours, postoperative pain at injection area at 6, 24 and 48 hours and analgesic intake after single-visit root canal treatment.

Conditions

  • Symptomatic Irreversible Pulpitis

Interventions

DRUG

Aceclofenac

Aceclofenac 100 mg tablet given one hour before starting the root canal treatment

OTHER

Placebo

Placebo tablet given one hour before starting the root canal treatment

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Nermeen A Abbas, Postgraduate · Cairo University

  • Suzan AW Amin, PhD · Cairo University

  • Shaimaa Gawdat, PhD · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2017-07-31
Completion
2017-07-31

Countries

  • Egypt

Study Locations

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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 NCT03335007 on ClinicalTrials.gov