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A study on the effect of bupivacaine liposomes for thoracic paravertebral block on postoperative cellular immune function and pain in patients undergoing thoracoscopic radical resection for lung cancer

The effect of bupivacaine liposomes on postoperative cellular immune function and pain in patients undergoing thoracoscopic radical resection of lung cancer undergoing thoracic paravertebral block: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094453
Enrollment
Unknown
Registered
2024-12-23
Start date
2024-12-28
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

Pulmonary malignant tumor

Interventions

Liposomebupivacaine Group(LB Group):Under ultrasound guidance, unilateral paravertebral block was performed by injecting 15ml of bupivacaine liposomes (a 10ml: 133mg bupivacaine liposome diluted with
Bupivacaine Hydrochloride Group(BH Group):Under ultrasound guidance, unilateral paraspinal block was performed by injecting 15ml of 0.25% bupivacaine (a 5ml mixture of 0.75% bupivacaine and 25ml steri
Control Group(C Group):None

Sponsors

The Second Hospital & Clinical Medical School, Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.No gender restrictions, age>= 18 years old; 2.ASA= 27 points; 4. This study has been approved by the Medical Ethics Committee of our hospital, and patients have signed informed consent forms; 5. Patients diagnosed with non-small cell carcinoma of type I, II, or IIIa who are planning to undergo thoracoscopic assisted (single port) radical resection for lung cancer.

Exclusion criteria

Exclusion criteria: 1.Allergy to anesthetic drugs, significant functional impairment of vital organs such as respiration, circulation, liver and kidney before surgery; 2.Preoperative examination results indicate distant metastasis; 3. Preoperative radiotherapy, chemotherapy, and hormone therapy; 4.Long term use of sedatives and analgesics, and perioperative blood transfusion therapy; 5. Participated in other studies within the past three months and suffered from other malignant tumors;6.Those who are not suitable for thoracic paravertebral nerve block, such as those with back infections, spinal deformities, etc; 7.Those who have difficulty completing follow-up or have various factors that affect compliance;8.Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Cellular immune related indicators;Blood glucose;Related complications and adverse reactions: nausea, vomiting, fever, constipation, dizziness, headache, insomnia, itching, pneumothorax, atelectasis;

Secondary

MeasureTime frame
Visual Analogue Scale(VAS);Intraoperative hemodynamic indicators;Incidence of vascular adverse events in the surgical center;Intraoperative use of vasoactive drugs;Intraoperative sedative dosage;Intraoperative remifentanil dosage;15 Quality of Recovery Scale (QoR-15) Score;First press time and cumulative press frequency of postoperative analgesia pump;Consumption of sufentanil 24 hours and 24-48 hours after surgery;The number of people in need of remedial analgesia, the frequency of remedial analgesia, and the type and dosage of remedial analgesia drugs;

Countries

China

Contacts

Public ContactWang Yingbin

The Second Hospital & Clinical Medical School, Lanzhou University

wangyingbin6@163.com+86 138 9313 3264

Outcome results

None listed

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