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Study for the safety and effectiveness of the ultrasound-guided mid-point transverse process to pleura block for uniportal video-assisted thoracoscopic surgery

Study for the safety and effectiveness of the ultrasound-guided mid-point transverse process to pleura block for uniportal video-assisted thoracoscopic surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027618
Enrollment
Unknown
Registered
2019-11-21
Start date
2019-11-30
Completion date
Unknown
Last updated
2019-11-25

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

Conditions

Postoperative analgesia

Interventions

Group 1:Paravertebral nerve block
blank control group:No treatment
Group 2:MTP block

Sponsors

The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing uniportal video-assisted thoracoscopic surgery; 2. Aged 18 -65 years; 3. ASA grade I-III grade; 4. BMI 19-28kg/m2.

Exclusion criteria

Exclusion criteria: 1. Patients after thoracic vertebrae surgery; 2. Severe liver and kidney function injury; 3. Coagulation dysfunction; 4. Those who are unable to cooperate with mental illness; 5. Alcohol, opioid addicts.

Design outcomes

Primary

MeasureTime frame
The VAS scores during a cough and rest;—

Countries

China

Contacts

Public ContactXhen Xu

The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China

vanesth@163.com+86 18326108020

Outcome results

None listed

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