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Ultrasound-guided thoracic paravertebral and rhomboid intercostal multipoint nerve blocks on postoperative recovery after porous thoracoscopic surgery: a non-inferiority study

Ultrasound-guided thoracic paravertebral and rhomboid intercostal multipoint nerve blocks on postoperative recovery after porous thoracoscopic surgery: a non-inferiority study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073661
Enrollment
Unknown
Registered
2023-07-18
Start date
2024-01-04
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

postoperative pain.

Interventions

Thoracic paravertebral nerve block group.:Under the guidance of ultrasound, a thoracic paravertebral nerve block was performed at the T5 and T7 levels along the midline of the trunk. A total of 20 ml
rhomboid intercostal nerve block.:Under the guidance of ultrasound, a rhomboid intercostal nerve block was performed at the T5 and T7 levels along the midline of the trunk. A total of 20 ml of 0.5% ro

Sponsors

Affiliated Hospital of Jiaxing University (Jiaxing First Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who scheduled for unilateral three-port thoracoscopic lung segmental resection; 2. Aged 18-80 years; 3. ASA Level I-III.

Exclusion criteria

Exclusion criteria: 1. Abnormal heart, lung, liver, kidney, and coagulation functions; 2. Intended block area infection, severe nerve damage to the block side limb; 3. Patients with a history of chronic pain, taking analgesics, psychiatric medications, radiation and chemotherapy, and contraindications to non-steroidal anti-inflammatory drugs; 4. Patients with allergies to local anesthetics such as lidocaine, ropivacaine, and general anesthetics; 5. Patients and their families who refuse surgical anesthesia and are unable to complete the survey questionnaire.

Design outcomes

Primary

MeasureTime frame
24h postoperative resting pain numeric score (NRS) mean difference between the groups;

Secondary

MeasureTime frame
the quality of recovery-40;pain numeric score mean difference between the groups;The dosage of sufentanil and the number of rescue analgesia administrations within 48 hours postoperatively.;All postoperative complications.;

Countries

China

Contacts

Public ContactMingzi An

Affiliated Hospital of Jiaxing University

anmingzizi@163.com+86 180 3519 3080

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026