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Analgesic Efficacy and Safety of a Multimodal Analgesic Regimen Combining Intercostal Nerve Block with Perioperative Oral Analgesics After Thoracoscopic Surgery

Analgesic Efficacy and Safety of a Multimodal Analgesic Regimen Combining Intercostal Nerve Block with Perioperative Oral Analgesics After Thoracoscopic Surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121789
Enrollment
Unknown
Registered
2026-04-02
Start date
2026-04-02
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

Post-thoracoscopic surgery pain

Interventions

Experimental intervention group:Multimodal analgesia with intercostal nerve block combined with perioperative oral analgesics
Control intervention group:Postoperative patient-controlled intravenous opioid analgesia

Sponsors

Gansu Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years, regardless of gender; 2. Meet the indications for pulmonary surgery and scheduled to undergo thoracoscopic lobectomy/segmentectomy/partial pulmonary resection; 3. Scheduled to receive video-assisted thoracoscopic surgery (VATS); 4. Complete clinical data and meet the indications for anesthesia and surgery; 5. No mental illness or cognitive dysfunction, able to cooperate with all pain and recovery assessments; 6. American Society of Anesthesiologists (ASA) physical status classification ? or ?; 7. Voluntarily participate in this study and sign the written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Hypersensitivity to any component of the study drugs (bupivacaine colloid, celecoxib, paracetamol, tramadol); 3. Complicated with hemorrhagic diseases or severe coagulation dysfunction; 4. Preoperative history of chronic pain or intercostal neuralgia; 5. History of opioid abuse, alcohol or drug dependence; 6. Conversion to open thoracotomy during surgery for any reason; 7. Placement of >= 2 thoracic closed drainage tubes after surgery; 8. Patients judged by the investigators to have other clinical conditions unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Postoperative opioid consumption (converted to morphine equivalent);Visual Analogue Scale (VAS) pain score;Quality of Recovery-15 (QOR-15) score;Richards-Campbell Sleep Questionnaire (RCSQ) score;

Secondary

MeasureTime frame
Prince-Henry pain score;Times of rescue analgesia as per medical advice;Time to first ambulation after surgery;Incidence of postoperative adverse events and complications;

Countries

China

Contacts

Public ContactYunjiu Gou

Gansu Provincial Hospital

775170118@qq.com+86 138 9335 4835

Outcome results

None listed

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