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The effect of intrathoracic injection of different concentrations of ropivacaine on deep respiratory pain after VATS surgery

The effect of intrathoracic injection of different concentrations of ropivacaine on deep respiratory pain after VATS surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098724
Enrollment
Unknown
Registered
2025-03-12
Start date
2024-12-03
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Postoperative Pain

Interventions

0.25% Ropivacaine group:After extubation, the postoperative patient was injected with 15ml of ropivacaine at a concentration of 0.25% through a thoracic catheter
0.5% Ropivacaine group:After extubation, the postoperative patient was injected with 15ml of ropivacaine at a concentration of 0.5% through a thoracic catheter
0.9% NS group:After extubation, the postoperative patient was injected with 15ml of physiological saline through a thoracic catheter

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age between 18-60 years old, ASA grade II-III, BMI18.5-23.9kg/m^2, Lung cancer patients undergoing single port VATS treatment in our hospital.

Exclusion criteria

Exclusion criteria: Patients who are under 18 years old or over 60 years old, have an ASA grade greater than III, a BMI less than 18.5kg/m^2 or greater than 23.9kg/m^2, are allergic to ropivacaine, have obvious chest deformities, have recent lung infections, have a history of lung surgery, chronic pain, are currently using opioid drugs, alcohol or opioid drug dependence, have severe liver and kidney dysfunction, mental illness, and cannot complete digital rating scale measurements. Patients who need to undergo thoracotomy due to surgical needs.

Design outcomes

Primary

MeasureTime frame
Number of cases of postoperative deep breathing pain;

Secondary

MeasureTime frame
The first occurrence time of postoperative deep breathing pain;NRS scores at 4, 8, 12, 24, and 48 hours postoperatively;The frequency and total amount of postoperative salvage analgesia with tramadol;The incidence of postoperative pulmonary complications;The incidence of postoperative local anesthetic adverse reactions;

Countries

China

Contacts

Public ContactGangming Wu

The First Affiliated Hospital of Chongqing Medical University

317419592@qq.com+86 151 7883 2887

Outcome results

None listed

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