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MK0686 in Postsurgery Dental Pain (0686-002)

NCT00533403 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 114

Last updated 2015-06-26

No results posted yet for this study

Summary

To compare the pain relieving effect of MK0686 to placebo or ibuprofen after dental surgery.

Conditions

  • Pain, Postoperative

Interventions

DRUG

MK0686

Sponsors & Collaborators

Principal Investigators

  • Medical Monitor · Merck Sharp & Dohme LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-07-31
Primary Completion
2004-11-30
Completion
2004-11-30

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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 NCT00533403 on ClinicalTrials.gov