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A randomized controlled trial of ropivacaine analgesia after thoracoscopic lung cancer resection

A randomized controlled trial of ropivacaine analgesia after thoracoscopic lung cancer resection

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060661
Enrollment
Unknown
Registered
2022-06-06
Start date
2022-05-23
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

Lung cancer

Interventions

The thoracic analgesia group:Pleural analgesia by Ropivacaine
The intercostal analgesia group:Intercostal analgesia by Ropivacaine
The PCIA group:PCIA
The paravertebral analgesia group:Paravertebral analgesia by Ropivacaine

Sponsors

Army Medical Center of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. 18-80 years old, gender is not limited; 2. Pulmonary nodules are mainly composed of ground glass (>50%), with a diameter of <= 2cm, and thoracoscopic segmentectomy + lymph node sampling is planned; 3. Able to tolerate surgery, with good cardiopulmonary and other organ function; 4. The subjects were able to read and fully understand the relevant contents of the informed consent form, and signed the informed consent form at the same time.

Exclusion criteria

Exclusion criteria: 1. Allergy to ropivacaine; 2. It is planned to perform multiple segmentectomy or combined lobectomy at the same time; 3. The lesions are dominated by solid components, or the possibility of invasive lung cancer is considered; 4. Patients with previous history of tuberculous pleurisy or thoracic surgery on the same side of surgery, considering extensive adhesion of the pleural cavity; 5. Liver and kidney insufficiency; 6. Refused to participate in clinical trials; 7. Severe hypertension or other contraindications to flurbiprofen use.

Design outcomes

Primary

MeasureTime frame
Pain Visual Scale Score;Postoperative complications;

Secondary

MeasureTime frame
Leukocyte;Thoracic drainage volume;Interleukin-6;Number of pain medication used;The removal time of Drainage tube;

Countries

China

Contacts

Public ContactMeng Shenglan

Army Medical Center of PLA

mengshenglan-hx@163.com+86 15213143384

Outcome results

None listed

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