Comparison of Local Anesthetic Infusion Pump Versus Depofoam Bupivacaine for Pain Management

Completed · Phase 4

Conditions studied: Pain, Postoperative

In brief

Effective post surgical pain control in patients undergoing unilateral deep inferior epigastric perforator (DIEP) free flap reconstruction.

Key facts

Study ID

NCT04284930

Run by

The Cleveland Clinic

People needed

21

Starts

2016-02-01

Expected to finish

2017-11-01

Last updated by the study team

2021-01-07

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Non pregnant women
• age 18 years or older
• scheduled to have unilateral DIEP flap breast reconstruction.
• Must have ASA physical status classification of 1,2, or 3

You may not qualify if…

• concurrent or recent medical condition that could interfere with study participation
• history of any of the following:
• hepatitis
• alcohol/substance abuse
• uncontrolled psychiatric disorders
• known allergy/ contraindication to any of the following:
• amide-type local anesthetics
• opioids
• propofol
• Body weight of less than 50 kg
• have participated in another study involving an investigational medication with in the past 30 days
• taking analgesics, antidepressants, or glucocorticoids within the 3 days before surgery

Where it is running

• Cleveland Clinic Foundation — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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