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Dexketoprofen Trometamol in Postoperative Endodontic Pain

NCT02086097 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2014-05-07

No results posted yet for this study

Summary

The purpose of this study is to investigate the analgesic efficacy of multiple doses of Dexketoprofen Trometamol 25 mg on postoperative pain following emergency endodontic treatment in teeth with irreversible pulpitis, using as control Ibuprofen 600 mg and a placebo group.

Hypothesis:

Dexketoprofen trometamol when administered in multiple doses produces a greater effect to control postoperative pain after treating symptomatic irreversible pulpitis; in patients undergoing pulpotomy as an emergency procedure

Conditions

  • Irreversible Pulpitis

Interventions

DRUG

Dexketoprofen trometamol

25m of dexketoprofen (oral intake) every 8 hours

DRUG

Ibuprofen

600 mg of Ibuprofen (Oral Intake) every 8 hours

DRUG

PLACEBO

INACTIVE SUGAR PILLS

Sponsors & Collaborators

  • Daniel Chavarría Bolaños

    lead OTHER

Principal Investigators

  • Gisela Rodríguez, DDS · Universidad Autonoma San Luis Potosi

  • Amaury J Pozos-Guillen, PhD · Universidad Autonoma San Luis Potosi

  • Daniel Chavarria, PhD · Universidad Autonoma San Luis Potosi

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-08-31
Primary Completion
2014-04-30
Completion
2014-04-30

Countries

  • Mexico

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 NCT02086097 on ClinicalTrials.gov