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NCT00664690 Clinical Trial

Effect of Celecoxib on Transitional Pain After Outpatient Surgery

Pain Clinical Trial

Official title:
Effect of Celecoxib on Transitional Pain After Outpatient Surgery

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00664690
Other study ID # R-04-309
Secondary ID 10457
Status Withdrawn
Phase Phase 4
First received April 18, 2008
Last updated August 25, 2017

Study information
Verified date August 2017
Source Lawson Health Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Sixty adults having shoulder and forearm surgery will receive either placebo or celebrex started preoperatively and continued for 3 days. Rescue medications required as well as pain scores will be assessed using a patient diary to evaluate the effect of celebrex in controlling transitional pain

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients scheduled for elective ambulatory surgery of the shoulder

- ASA I - III

- Able to read English

- Male or female

Exclusion Criteria:

- Allergy to local anesthetic, Cox2, sulpha drug, acetaminophen or oxycodone

- Women who are pregnant or lactating and women of childbearing age and not following acceptable contraceptive precautions

- Any major medical or psychiatric problem

- Those with a known history of narcotic dependence, abuse or chronic narcotic intake

- Patients with known history of peptic ulcer or GI bleeding in the past, ulcers, congestive heart failure, angina or previous heart attack, coagulation problems, venous thrombosis, kidney or liver disease or strokes

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• celebrex
400 mg celebrex given 1 hour preop and celebrex 200 mg BID postop
• placebo
placebo given preop and BID postop

Locations
Country Name City State
Canada St. Joseph's Health Care London Ontario

Sponsors (1)
Lead Sponsor Collaborator
Lawson Health Research Institute

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary visual analogue score for pain post-op period
Secondary severity of nausea post-op period
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