Endoscopy Clinical Trials

Clinical trials related to Endoscopy Procedure

Continuous Infusion Pump Versus Single Shot Peripheral Block for Pain Management After Same-day Orthopaedic Surgery

Status: Recruiting
Location: See location...
Intervention Type: Device, Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Objectives: The primary objective is to compare the effectiveness of postoperative infusion pain pump versus preoperative nerve block in reducing visual analog pain scores/numerical pain rating scale (VAS/NPRS) in the postoperative period. The second objective is to evaluate the requirement of narcotic and non-narcotic analgesic medications between the two groups. Hypotheses: Use of continuous infusion pain pump or single shot peripheral block will result in similar post-operative pain control after outpatient sports medicine surgical cases.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age 18 years or older

• ACL reconstruction

• Open shoulder labrum or rotator cuff surgery

• Arthroscopic rotator cuff repair

• Proximal or distal patellar realignment surgery

• Open knee arthrotomy cases - Inside out meniscus repair, OCA, MAT

Locations
United States
New Jersey
University Center for Ambulatory Surgery
RECRUITING
Somerset
Contact Information
Primary
Charles Gatt, MD
cjgatt85@gmail.com
732-537-0909
Time Frame
Start Date: 2026-01-01
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 80
Treatments
Experimental: Post-Operative: Continuous ropivacaine via Ambit pump
Postoperatively, infusion pump reservoirs will contain 0.20% ropivacaine and infused via the Ambit pump (8cc/hr for knees, 6cc/hr for shoulders).
Active_comparator: Pre-Operative: Liposomal bupivacaine (Exparel)
A single-shot of Liposomal Bupivicaine (Exparel) will be administered pre-operatively
Related Therapeutic Areas
Sponsors
Leads: Rutgers, The State University of New Jersey

This content was sourced from clinicaltrials.gov