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The postoperative analgesia effect of ultrasound guided vertebral nerve block combined with dexmedetomidine in thoracoscopic lobectomy.

The postoperative analgesia effect of ultrasound guided vertebral nerve block combined with dexmedetomidine in thoracoscopic lobectomy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17013034
Enrollment
Unknown
Registered
2017-10-19
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

Lung cancer

Interventions

General anesthesia group:General anesthesia(inducted with sufentanil 5ug/kg+etomidate 2mg/kg + cisatriptan 2mg/kg,maintained with propofol 2.5ug/ml+remifentanil 3 ng/ml)
Control group:Ropivacaine 10ml ultrasound guided for T5 vertebral nerve block (after induction, before surgery)
Dexmedetomedine group:Dexmedetomedine 1.0ug/kg+0.5% ropivacaine 10ml ultrasound guided for T5 vertebral nerve block (after induction, before surgery)

Sponsors

Suzhou Science & Technology Town Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who planned to accept Unilateral thoracoscopic lobectomy under general anesthesia; 2. aged 18-65 years; 3. ASA grade I-III; 4. without cardiac or pulmonary diseases such as sinoatrial bradycardia, Functional lesions of sinus node or severe arrhythmia, without chest deformity; 5. Patients themselves and whose relatives who are fully aware of this study and agree to take part.

Exclusion criteria

Exclusion criteria: 1. Patients who have underwent or are undergoing other kinds of clinical trials; 2. according to the physicians judgement, patients who may suffer greater risk in this study or their data cannot be collected sufficiently should be excluded; 3. patients whose surgeries were finished under other kinds of anesthesia instead of general anesthesia or patients whose surgeries were changed to conventional thoracotomy.

Design outcomes

Primary

MeasureTime frame
VAS scale;Ramsay sedation score;

Countries

China

Contacts

Public ContactWang Chen

Suzhou Science & Technology Town Hospital

wangchen1791@163.com+86 17715187003

Outcome results

None listed

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