Paravertebral Block vs no Block in Open Pancreaticoduodenectomy

• Status: Not yet recruiting
• Trial end date: 2024-12-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to compare intra and postoperative pain control between Paravertebral block vs no block in open pancreaticoduodenectomy. Length of stay, and complications will also be recorded. For this study the investigator plans to randomize to obtain objective data for clinical decisions and improve patient outcomes. Following surgery patients in both groups, data will be collected from the first 48 hours after surgery and at discharge.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Mayo Clinic
• Treatments: Ropivacaine

Criteria

Inclusion Criteria:

• Patients willing and have signed consent.

• Nonpregnant adults undergoing open pancreaticoduodenectomy via standard upper midline incision without contraindications to para vertebral block (PVB)

Exclusion Criteria:

• Not able or unwilling to sign consent.

• Currently pregnant or lactating.

• Patients with chronic pain, requiring daily opiate use at time of surgery.

• Patients intolerant of opiates, NSAIDS, acetaminophen or local anesthetics.