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The effect of paravertebral nerve block with liposomal bupivacaine combined with transversus abdominis plane block on the quality of postoperative recovery in patients undergoing thoracoabdominal laparoscopic radical resection of esophageal cancer: A randomized, controlled, double-blind trial

The effect of paravertebral nerve block with liposomal bupivacaine combined with transversus abdominis plane block on the quality of postoperative recovery in patients undergoing thoracoabdominal laparoscopic radical resection of esophageal cancer: A randomized, controlled, double-blind trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129218
Enrollment
Unknown
Registered
2026-08-01
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients who underwent combined thoraco-abdominal laparoscopic radical resection for esophageal tumors

Interventions

R group:Control group: Ropivacaine Hydrochloride Injection
L group:Experimental group: Liposomal Bupivacaine Injection

Sponsors

HenanCancerHospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age range: 45 - 75 years old; 2.no gender limitation; 3.American Society of Anesthesiologists (ASA) Physical Status Classification System Grade ? to ?; 4.Body mass index (BMI) 18.5 to 30.0 kg/m²; 5.Patients undergoing radical resection of esophageal cancer under general anesthesia via combined thoracoscopic and laparoscopic approach;

Exclusion criteria

Exclusion criteria: 1.Patients with a long history of chronic pain or opioid dependence preoperatively. 2.Patients with a history of allergy to local anesthetics or opioids. 3.Patients with contraindications to regional nerve blocks. 4.Patients who cannot cooperate with the study assessments due to cognitive or communication disorders.

Design outcomes

Primary

MeasureTime frame
Postoperative Recovery Quality;

Secondary

MeasureTime frame
Number of cases with postoperative rescue analgesia and the amount of rescue analgesic medication used;Postoperative adverse reactions and complications;Time to first ambulation and time to first flatus;Rest and activity NRS scores at 2, 12, 24, 48, and 72 hours postoperatively;Postoperative Sufentanil Consumption;

Countries

China

Contacts

Public ContactLu Xihua

HenanCancerHospital

hnlxh66@163.com+86 371 65588325

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026