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Effect of a Novel Ultrasound-Guided Intertransverse Process Block on Analgesia, Stress Response, and Postoperative Recovery in Patients Undergoing Thoracoscopic Radical Lung Cancer Surg

Effect of a Novel Ultrasound-Guided Intertransverse Process Block on Analgesia, Stress Response, and Postoperative Recovery in Patients Undergoing Thoracoscopic Radical Lung Cancer Surg

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113447
Enrollment
Unknown
Registered
2025-11-28
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Lung Cancer

Interventions

Intertransverse Process Block (ITPB) Group:Intertransverse Process Block
Paravertebral Block Group (TPVB Group):Paravertebral Block

Sponsors

Department of Anesthesia,Longyan First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Age 18-80 years; 2 ASA classification I-III; 3 According to the Clinical Practice Guidelines for Lung Cancer by the Chinese Medical Association (2023 edition), combined with clinical manifestations, imaging, and pathological examinations, the preoperative diagnosis of primary lung cancer is confirmed, and the patient meets the surgical indications for radical lung cancer surgery; 4 Elective unilateral thoracoscopic radical lung cancer surgery; 5 Meet ethical requirements, voluntarily agree, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1 History of previous chest surgery 2 Severe coagulation disorders 3 Infection at the puncture site 4 History of cognitive impairment or mental illness 5 History of chronic pain 6 Long-term use of analgesics or sedatives, or history of alcohol or drug abuse 7 Dysfunction of the heart, lungs, liver, or kidneys 8 Allergic to study drugs 9 Pregnant women

Design outcomes

Primary

MeasureTime frame
24hAUC;COR;QOR-15;Six-Minute Walk Test;Glu;IL-6;IL-10;CRP;

Secondary

MeasureTime frame
MAP;HR;SpO2;Plane;Number of times the pain pump was pressed within 24 hours;Fentanyl usage within 24 hours;24 hours Tramadol usage;complications;Time to remove the tracheal tube;Duration of chest tube placement;Hospitalization period;Satisfaction;Incidence of chronic pain 30 days post-surgery;

Countries

China

Contacts

Public ContactYunyun Tu

Department of Anesthesia,Longyan First Affiliated Hospital of Fujian Medical University

809186563@qq.com+86 182 5006 2603

Outcome results

None listed

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