Coscotransverse foramen block for perioperative analgesia in video- assisted thoracoscopic lobectomy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100041815

Enrollment

Unknown

Registered

2021-01-06

Start date

2021-01-08

Completion date

Unknown

Last updated

2021-03-30

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

Conditions

Video- assisted thoracoscopic lobectomy

Interventions

Costotransverse foramen block:Costotransverse foramen block

Erector spinal planeblock group:Thoracic vertebra erector spinal plane block

Paravertebral block group:Thoracic paravertebral block

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective thoracoscopic lobectomy under general anesthesia; 2. ASA I - III subjects, aged 18-65 years; 3. Patients with operation time of 1-3 hours.

Exclusion criteria

Exclusion criteria: 1. Patients with puncture site infection; 2. Anticoagulant subjects; 3. Morbidly obese subjects (BMI >= 40 kg / m2); 4. Subjects allergic to local anesthetics; 5. Subjects with severe heart and lung diseases; 6. Patients with liver and kidney dysfunction and neuropsychiatric diseases; 7. Patients with history of thoracic surgery.

Design outcomes

Primary

Measure	Time frame
Numeric rating scale (NRS);Dermatome of analgesia;	—

Secondary

Measure	Time frame
Rescue sufentanil and its does;Rescue analgesic and its does;Duration of the block procedure;Patients' satisfaction;Quality of life;Adverse effects;	—

Countries

China

Contacts

Public ContactJia Jiang

Beijing Chaoyang Hospital Affiliated to Capital Medical University

neighbor93918@126.com+86 13488858695

Outcome results

None listed

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