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Effectiveness of Ultrasound-guided Extrapleural block Analgesia for Minimally Invasive Thoracic Surgery :A Randomized Clinical Trial

Effectiveness of Ultrasound-guided Extrapleural block Analgesia for Minimally Invasive Thoracic Surgery :A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093300
Enrollment
Unknown
Registered
2024-12-02
Start date
2024-12-03
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Minimally Invasive Thoracic Surgery

Interventions

Group E (extrapleural block group):Ultrasound-guided midaxillary line horizontal injection was performed at 4/5 intercostal and 6/7 intercostal sites for extrapleural block
Group P (thoracic paravertebral block group):Thoracic paravertebral nerve block was performed in thoracic 4 paravertebral space and thoracic 6 paravertebral space under ultrasound guidance

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists ASA Grade I ~ III; 2. Elective patients who plan to undergo minimally invasive thoracic surgery; 3, age 18-65 years old; 4. The subjects voluntarily joined the study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Liver and kidney insufficiency; 2. Allergic to the drug to be used;3. History of chronic pain; 4. History of opioid dependence or opioid use >1 month; 5, dementia, language disorders or neuropsychiatric disorders can not cooperate with patients; 6. Patients with contraindications to regional anesthesia; 7. Patients who were accidentally converted to thoracotomy during minimally invasive thoracic surgery or were admitted to ICU for continued mechanical ventilation after surgery.

Design outcomes

Primary

MeasureTime frame
Dosage of sufentanil 24h after operation in two groups;

Secondary

MeasureTime frame
VAS score;First compression time for controlled analgesia;Quality of recovery 24 hours after surgery was assessed by QoR-15 questionnaire;Nerve block operation time T0, number of puncture;Drainage tube removal time;

Countries

CHINA

Contacts

Public Contactgaojuzheng

Shenzhen Second People's Hospital

616152719@qq.com+86 134 1849 2794

Outcome results

None listed

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