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Analgesic Preoperative/Postoperative Dexketoprofen Trometamol in Third Molar Surgery

NCT02380001 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2015-08-14

No results posted yet for this study

Summary

The purpose of the present investigation is to evaluate the effectiveness of the preoperative administration of Dexketoprofen Trometamol, employing the third molar surgery model, when compared to postoperative administration of the same drug. It was hypothesized that preoperative oral Dexketoprofen trometamol will reduce the intensity of pain by 30% after 8 hours of the surgery, when compared with post-operative administration.

Conditions

  • Postoperative Pain

Interventions

DRUG

Dexketoprofen trometamol

White round pill containing 25mg of Dexketoprofen will be administered either prior/after to third molar surgery.

DRUG

Preoperative control

white round pill containing 25mg of placebo will be administered prior/after to third molar surgery. The placebo pill is identical to active dexketoprofen, in size and color

Sponsors & Collaborators

  • Daniel Chavarría Bolaños

    lead OTHER

Principal Investigators

  • Amaury Pozos, PhD · Universidad Autónoma de San Luis Potosí

  • Vicente Esparza, Resident · Universidad Autónoma de San Luis Potosí

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2015-08-31
Completion
2015-08-31

Countries

  • Mexico

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 NCT02380001 on ClinicalTrials.gov