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Efficacy of combined erector spinae plane block and thoracic paravertebral block for analgesia in thoracoscopic pneumonectomy: a prospective, randomized clincal trial

Efficacy of combined erector spinae plane block and thoracic paravertebral block for analgesia in thoracoscopic pneumonectomy: a prospective, randomized clincal trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037688
Enrollment
Unknown
Registered
2020-08-30
Start date
2020-09-15
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Pain in thoracoscopic pneumonectomy

Interventions

E group:ESP block
T group:TVP block
ET group:combined ESP block and TVP block

Sponsors

The Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. The patients of both sexes, aged 18-65 years, ASA 1-3 grade; 2. Patients who voluntarily accept the use of postoperative analgesia pump; 3. Patients who underwent thoracoscopic lobectomy / pulmonary wedge surgery / lung artillery surgery; 4. Patients who volunteer and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with allergic history of local anesthetics or NSAIDs; 2. Patients with infection or other contraindications near the puncture site; 3. Patients with chronic pain history or frequent use of analgesics; 4. Patients with mental cognitive impairment and communication disorder.

Design outcomes

Primary

MeasureTime frame
pain score at rest at 2 h post-surgery;

Secondary

MeasureTime frame
qualtiy of recovery;Patient satisfaction score;length of postoperative hospital stay;time to first opioid administration;opioid consumption in the first 24 hours postoperatively;incidence of operative hypotension;postoperative pulmonary complications;Chronic postoperative pain;The distribution pattern of local anesthesia;dose of intraoperative anesthetic usage;pain scores during the first 24 h post-surgery;duration of chest tube;sensory blockade at anterolateral thoracic wall;

Countries

China

Contacts

Public ContactYe zhang

The Second Affiliated Hospital of Anhui Medical University

zhangye_hassan@sina.com+86 551-63869485

Outcome results

None listed

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