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Not Yet RecruitingNCT06405724

Comparison of the Ultrasound-guided Paravertebral Nerve Block With Liposomal Bupivacaine Versus Ropivacaine for Post-Surgical Pain After Video-Assisted Thoracoscopic Surgery

Comparison of the Ultrasound-guided Paravertebral Nerve Block With Liposomal Bupivacaine Versus Ropivacaine for Post-Surgical Pain After Video-Assisted Thoracoscopic Surgery:A Single-Center, Prospective, Randomized, and Controlled Trial

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
84 (estimated)
Sponsor
Feng Gao · Academic / Other
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Not accepted

Summary

Prospective, randomized, and controlled trial to compare the postoperative pain management of paravertebral nerve block with liposomal bupivacaine to ropivacaine in patients undergoing elective thoracoscopic surgery.

Detailed description

The objective of this study is to validate the analgesic efficacy of liposomal bupivacaine (LB) compared with ropivacaine when injected for paravertebral nerve block (PVB) for video-assisted thoracoscopic surgery (VATS). We hypothesize that LB will be superior to ropivacaine in terms of postoperative pain control following VATS. The primary outcome of this study will be NRS pain scores for resting pain and NRS pain scores for cough pain 24 hours following surgery. Secondary outcomes will include pain scores over the first 120 hours following surgery, opioid consumption, opioid-related adverse events, block-related adverse events, time of first getting out of bed, catheter indwelling time, postoperative hospitalization time, patient satisfaction, and chronic pain at 1, 3, and 6 months after surgery.

Conditions

Interventions

TypeNameDescription
DRUGLiposomal bupivacaine133mg LB 20mL thoracic paravertebral nerve block
DRUGRopivacaine0.5% ropivacaine 20mL thoracic paravertebral nerve block

Timeline

Start date
2024-05-10
Primary completion
2025-12-21
Completion
2025-12-21
First posted
2024-05-08
Last updated
2024-05-08

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06405724. Inclusion in this directory is not an endorsement.