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Effect of dexmedetomidine on postoperative recovery of patients undergoing thoracoscopic resection of pulmonary lesions

Effect of dexmedetomidine on postoperative recovery of patients undergoing thoracoscopic resection of pulmonary lesions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056101
Enrollment
Unknown
Registered
2022-02-01
Start date
2022-02-01
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

pulmonary nodule

Interventions

Dexmetomidine group:Dexmedetomidine 0.25 ug/kg/h intravenous pumping for 9 hours, 9: 00 p.m. the day after surgery to 6: 00 a.m. the next day
Saline group:0.9% Sodium Chloride Injection 3 ml/h intravenous pumping for 9 hours, 9: 00 p.m. the day after surgery to 6: 00 a.m. the next day

Sponsors

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.The patients agreed to participate in this research and signed the informed consents; 2.ASA Physical condition I-III; 3.Age from 18 to 65 years old (including 18 and 65); 4.Patients scheduled for single-site thoracoscopic resection of pulmonary lesions (wedge, segmental, lobectomy) under general anesthesia.

Exclusion criteria

Exclusion criteria: 1.The subjects and their families refuse to complete the clinical study; 2.Known to be allergic to research drug; 3.Pathological sinus syndrome, clinically significant sinus bradycardia, or secondary or higher heart block without pacemaker; 4.Severe liver dysfunction (Child-Pugh GRADE C) or severe renal failure (requiring dialysis); 5.Preoperative history of endocrine diseases, chronic lung diseases, immune diseases and respiratory tract infections, and abnormal coagulation; 6.Serious cardiac duct adverse events occurred during operation; 7.Other serious adverse events occurred after surgery, such as septic shock and acute renal failure; 8.Patients with a history of long-term use of analgesic sedation, psychotropic drugs, drug addiction and allergy to narcotic drugs; 9.A past history of schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis; 10.If a physician or investigator violates the principles of study design during a clinical study, the ETHICS committee will terminate or suspend the clinical study.

Design outcomes

Primary

MeasureTime frame
Pittsburgh Sleep Quality Index, PSQI;Six-minute walk test;

Secondary

MeasureTime frame
Inflammatory biomarkers;Dosage of analgesic drugs;EuroQol five dimensions questionnaire;Numerical rating scale, NRS;

Countries

China

Contacts

Public ContactBingbing Li

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School

icecolor@163.com+86 15850521974

Outcome results

None listed

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