Celecoxib Japan Observational Study for the Patients With Acute Pain

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

784 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-07-31

Study Completion Date

2013-04-30

Brief Summary

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This study is to assess the safety and efficacy of celecoxib on the pain relief from acute pain.

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Detailed Description

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Patients with traumatic pain, post-surgical and tooth extract pain will be included in this study. Patients will receive Celecoxib for 2 weeks and the efficacy on pain relief and the safety will be evaluated.

Conditions

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Patients With Traumatic Pain, Post-surgical Pain and Tooth Extract Pain

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Celecox group

Celecoxib

Intervention Type DRUG

oral

Interventions

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Celecoxib

oral

Intervention Type DRUG

Other Intervention Names

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Celecox

Eligibility Criteria

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Inclusion Criteria

* Patients with traumatic pain, post-surgical pain and tooth extract pain

Exclusion Criteria

* Hyperreactive to sulfonamide
* Aspirin asthma patients
* Peptidic ulcer patients
* Serious liver disease patients
* Serious kidney disease patients
* Serious heart failure patients
* End of pregnancy

Eligible Sex

ALL

Accepts Healthy Volunteers

No