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Combined general anesthesia with different volumes of ropivacaine intertransverse block in thoracoscopic pulmonary resection

Combined general anesthesia with different volumes of ropivacaine intertransverse block in thoracoscopic pulmonary resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095225
Enrollment
Unknown
Registered
2025-01-03
Start date
2025-01-03
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

None

Interventions

Group A:Intertransverse process block with 0.3 ml/kg of ropivacaine 0.375%
Group B:Intertransverse process block with 0.4 ml/kg of ropivacaine 0.375%
Group C:Intertransverse process block with 0.5 ml/kg of ropivacaine 0.375%

Sponsors

The First Affiliated Hospital of Gannan Medical University, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1)American Society of Anesthesiologist physical status Classification I-III; (2)Patients aged 18-75 years old who plan to elective thoracoscopic lobectomy/segmental lung resection at our hospital; (3)Agree to participate in the study and be able to understand the relevant assessment content; (4)Height 145-175 cm; (5)BMI 18.5-28 kg/m^2 .

Exclusion criteria

Exclusion criteria: (1) Contraindications to regional nerve block, including but not limited to abnormal coagulation function, skin infection at the block site, and allergy to local anesthetic drugs; (2) Presence of severe organ dysfunction, including but not limited to renal dysfunction (creatinine >442umol/L or renal replacement therapy), hepatic dysfunction (Child-Pugh class C), central or peripheral system diseases and other severe cardiopulmonary diseases; (3) History of chronic pain, those taking opioids, hormones or non-steroidal drugs for a long period of time; (4) Patients who have participated in other studies.

Design outcomes

Primary

MeasureTime frame
Incidence of intraoperative hypotension (hypotension defined as MAP<65mmHg or blood pressure drop of more than 30% from baseline for more than 1 minute);

Secondary

MeasureTime frame
Skin sensory block segment 20min after completion of block;Blood pressure and heart rate at different time points;The occurrence of hypotension at different time during operation;Intraoperative blood gas analysis at different time points (before induction of anesthesia, 1 h into surgery, at the end of surgery);Total intraoperative and postoperative opioid use;Total norepinephrine dosage and duration of use;Duration of surgery;Intraoperative infusion volume;Intraoperative bleeding;RASS scores at different postoperative time points (5 min postoperatively, 10 min postoperatively, 15 min postoperatively, 20 min postoperatively, 25 min postoperatively, 30 min postoperatively);Incidence of agitation during awakening;Postoperative tracheal tube removal time;Anesthesia recovery time;VAS scores of rest and activity at different time points after surgery (2h, 4h, 8h, 12h, 24h, 48h);The time of first PCA and the number of rescue analgesia in 48h after surgery;Rehabilitation quality scores before surgery and 24 and 48 hours after surgery (QoR-15);Postoperative nausea and vomiting, puncture site infection, itching and other adverse events;Postoperative drain removal time;time to first ambulation after surgery;time to diet after surgery;time to exhaust after surgery;

Countries

China

Contacts

Public ContactZhan Lifang

The First Affiliated Hospital of Gannan Medical University

zhanlifangzouping@163.com+86 158 7973 1530

Outcome results

None listed

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