Sponsor:
Wayne State University
Code:
NCT05090761
Conditions
Post Operative Pain, Acute
Eligibility Criteria
Sex: All
Age: 18 - 70+
Healthy Volunteers: Not accepted
Interventions
Bupivacaine 0.25% Injectable Solution
Bupivacaine 0.25% Injectable Solution, Magnesium Sulfate 150 mg
Bupivacaine 0.25% Injectable Solution, Magnesium Sulfate 150 mg, Buprenorphine 300 mcg
Brief summary:
Conditions
Post Operative Pain, Acute
Study ID
NCT05090761
Start date
Oct 12, 2021
Status verified date
Oct, 2021
Completion date
Oct, 2022
Anticipated
Primary completion date
Oct, 2022
Anticipated
Eligibility Criteria
Sex: All
Age: 18 - 70+
Healthy Volunteers: Not accepted
Enrollment
120 participants
Anticipated
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary purpose
Supportive Care
Arms
active comparator: SAPB
active comparator: SAPB with Mg
active comparator: SAPB with Mg and Buprenorphine
Interventions
Bupivacaine 0.25% Injectable Solution
Bupivacaine 0.25% Injectable Solution, Magnesium Sulfate 150 mg
Bupivacaine 0.25% Injectable Solution, Magnesium Sulfate 150 mg, Buprenorphine 300 mcg
Primary outcome measure
Central contacts
Locations
St. Joseph Mercy Oakland Hospital
Recruiting
Pontiac, Michigan, United States, 48341
Contacts
Lena Anderson
248-858-6068Sponsor
Wayne State University
Last update posted
Oct 25, 2021
Last verified
Oct, 2021
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Wayne State University on 2021-10-25.