Comparison of Tramacet Versus Percocet in Post Surgical Patients

• Register: ClinicalTrials.gov
• Last refreshed on: 12 December 2020
• Main ID: NCT02361567
• Date of registration: 06/02/2015
• Prospective Registration: Yes
• Primary sponsor: Lawson Health Research Institute
• Public title: Comparison of Tramacet Versus Percocet in Post Surgical Patients
• Scientific title: Comparison of Tramacet Versus Percocet in Post Surgical Patients
• Date of first enrolment: April 2015
• Target sample size: 160
• Recruitment status: Completed
• URL: https://clinicaltrials.gov/show/NCT02361567
• Study type: Interventional
• Study design: Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Triple (Participant, Care Provider, Outcomes Assessor).
• Phase: Phase 4

Countries of recruitment

Canada

Contacts

• Name: Collin Clarke, MD
• Affiliation: Lawson Health Research Institute

Key inclusion & exclusion criteria

Inclusion Criteria age 18-65

opioid naïve

postoperative from mild to moderate pain risk surgery (surgery in which patients do not
generally require a patient controlled Analgesic pump post-operatively, or require post
operative analgesia beyond 14 days)

Exclusion Criteria:

Patients on Opioids

Children < 18 years

Elderly

Pregnancy

Language barrier

Past medical history of psychosis

Coexisting use of anti-depressants

American Society of Anesthesia Risk Score >3

Known allergy to opioid or acetaminophen



Age minimum: 18 Years
Age maximum: 65 Years
Gender: All

Health Condition(s) or Problem(s) studied

Post Operative Pain

Intervention(s)

Drug: Percocet

Drug: Tramacet

Primary Outcome(s)

Sought Second Prescription [Time Frame: 6 weeks post-operative]

Secondary ID(s)

103278

Source(s) of Monetary Support

Please refer to primary and secondary sponsors