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Comparison of Analgesic Effects of Intercostal Nerve Blockade via Different Approaches after Thoracoscopic Surgery: A Randomized Controlled Study

Comparison of Analgesic Effects of Intercostal Nerve Blockade via Different Approaches after Thoracoscopic Surgery: A Randomized Controlled Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114899
Enrollment
Unknown
Registered
2025-12-18
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-08-24

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

Conditions

Acute pain

Interventions

Experimental group:The surgeon performed percutaneous intercostal nerve block at the 2nd to 6th intercostal spaces of the patient.
Control group:The surgeon performed intercostal nerve block in the patient's 2nd to 6th intercostal spaces within the thoracic cavity.

Sponsors

The People's Hospital of Leshan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=18 years old; 2.Planned for elective thoracoscopic pulmonary/segmental/wedge resection surgery; 3.ASA classification: I-III grades; 4.Voluntary signing of the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Has a history of chronic pain disorders; 2.Patients with allergy to local anesthetics; 3.BMI>=30kg/m^2; 4.Intellectual or mental disorders, making it impossible to cooperate with the patient; 5.Patients who refuse to sign the consent form;

Design outcomes

Primary

MeasureTime frame
The VAS pain score of the patient 48 hours after the operation;

Secondary

MeasureTime frame
Compare the postoperative rescue doses of opioid drugs in the two groups;Compare the postoperative hospital stay days of the two groups and the total cost from the start of the surgery to discharge.;The QOR-15 scores from the first day after the surgery to the third day.;The success rates and blocking times of intercostal nerve block in the two groups;The VAS pain scores of the two groups of patients at 24 hours and 72 hours after surgery;

Countries

China

Contacts

Public ContactLin Hongyan

The People's Hospital of Leshan

xiaosa0801@163.com+86 833 2119487

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026