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The effect of bupivacaine liposome thoracic paravertebral nerve block on the postoperative recovery quality of patients undergoing bariatric surgery

The effect of bupivacaine liposome thoracic paravertebral nerve block on the postoperative recovery quality of patients undergoing bariatric surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120917
Enrollment
Unknown
Registered
2026-03-23
Start date
2026-03-23
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bariatric surgery

Interventions

Group B (bupivacaine liposome group):Paravertebral nerve block with liposomal bupivacaine
Group L(ropivacaine group):Paravertebral nerve block with ropivacaine

Sponsors

Zhengzhou Central Hospital Affiliated to Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Age range: 18 - 55 years old. ASA classification: I - III. BMI: 28 - 45 kg/m^2. Patients scheduled for laparoscopic sleeve gastrectomy.

Exclusion criteria

Exclusion criteria: 1. Blood diseases or coagulation disorders; 2. Presence of mental or neurological disorders; 3. Allergy to local anesthetics or analgesics; 4. Renal or liver dysfunction; 5. Cardiac conduction block; 6. Unstable coronary artery disease; 7. NYHA classification of heart function 3-4; 8. Pregnancy or planning to get pregnant; 9. Severe alcoholism or long-term use of analgesics due to chronic pain.

Design outcomes

Primary

MeasureTime frame
The QOR-15 score at 24 hours after the operation;

Secondary

MeasureTime frame
The QOR-15 score at 48 hours postoperatively;Numerical Rating Score;Morphine consumption;The incidence of postoperative adverse reactions;

Countries

China

Contacts

Public ContactPengfei Wang

Department of Anesthesiology and Perioperative Medicine, Zhengzhou Central Hospital Affiliated to Zhengzhou University

854892658@qq.com+86 159 3718 4246

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 4, 2026