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Effects of lidocaine and dexmedetomidine on perioperative tumor metastasis markers and inflammatory markers in patients undergoing thoracoscopic lung cancer resection

Effects of lidocaine and dexmedetomidine on perioperative tumor metastasis markers and inflammatory markers in patients undergoing thoracoscopic lung cancer resection

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050796
Enrollment
Unknown
Registered
2021-09-04
Start date
2022-07-21
Completion date
Unknown
Last updated
2022-08-23

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

Conditions

lung cancer

Interventions

Control group:Intravenous pumping 0.9%NS
Lidocaine group:Intravenous pumping lidocaine
Dexmedetomidine group:Intravenous pumping dexmedetomidine
Lidocaine combined with dexmedetomidine group:Intravenous pumping lidocaine and dexmedetomidine

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 80 years; 2. Patients undergoing elective thoracoscopic resection of lung cancer; 3. Normal liver and kidney function; 4. The ASA classification is I to III; 5. Patients with lung cancer without distant dissemination (clinical stage <=II); 6. Consent to receive postoperative controlled analgesia and intraoperative intercostal nerve block; 7. Willing to accept long-term follow-up.

Exclusion criteria

Exclusion criteria: 1. Preoperative neoadjuvant chemotherapy or radiotherapy; 2. Pregnant women; 3. Allergic to lidocaine, ropivacaine, sufentanil, rocuronium and other anesthetic drugs; 4. Previous long-term treatment with beta-blockers; 5. There was preoperative coagulation dysfunction; 6. Preoperative severe heart disease (NYHA cardiac function grade >= III); 7. Severe renal insufficiency (serum creatinine > 118mg/dL) or renal replacement therapy; 8. Severe liver insufficiency (modified Child-Pugh grade C); 9. Preoperative acute infection is not well controlled; 10. Poor preoperative glycemic control (FBP over 3.9-13.8mmol/L); 11. Opioid abuse; 12. Mental health problems or cognitive impairment; 13. Patients with a history of epilepsy and taking medication; 14. Chronic inflammatory or autoimmune disease or previous long-term use of glucocorticoids or other inflammatory immunosuppressive therapy; 15. Patients with other anesthesia or surgery contraindications; 16. The patient refused to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Myeloperoxidase (MPO), a specific index of neutrophils extracellular trapping net in serum ;

Secondary

MeasureTime frame
Citrullinated histone (H3Cit), a specific index of neutrophils extracellular trapping net in serum;Tumor progression and metastasis related markers (VEGF-A, MMP-3, MMP-9) in serum;VAS scores at 24, 48, and 72 hours after operation at rest or on movement ;Qor-40 scores at 1, 2, and 3 days after surgery;Additional analgesic timepoint and opioid use were required for the first time after surgery;Gastrointestinal first exhaust, defecation time;Postoperative drainage tube removal time;All-cause mortality 30 days after surgery;Readmission rate due to complications 30 days after surgery;Length of stay;

Countries

China

Contacts

Public ContactWang Zhiping

Affiliated Hospital of Xuzhou Medical University

zhpsqxt@163.com+86 13338787071

Outcome results

None listed

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