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Effects of opioid-free anesthesia on hemodynamics and postoperative cognitive function in elderly patients undergoing thoracoscopic surgery: a randomized controlled trial

Effects of opioid-free anesthesia on hemodynamics and postoperative cognitive function in elderly patients undergoing thoracoscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092239
Enrollment
Unknown
Registered
2024-11-12
Start date
2024-11-28
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Postoperative cognitive dysfunction

Interventions

F:Induction of anesthesia: propofol 1.5-2.0 mg-kg-1, esketamine 0.4 mg-kg-1. Rocuronium bromide 0.6 mg-kg-1. Anesthesia maintenance: esketamine 0.1-0.2 mg-kg-1-h-1 and propofol 4-10 mg-kg-1-h-1 admini
C:Induction of anesthesia: propofol 1.5-2.0 mg-kg-1, sufentanil 0.4 µg-kg-1. Rocuronium bromide 0.6 mg-kg-1 was injected. Anesthesia maintenance: remifentanil 5-10 µg-kg-1-h-1 and propofol 4-10 mg-kg-

Sponsors

Liaoning Cancer Hospital & Institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients aged =65 years, of either sex, who were to undergo thoracoscopic lobectomy; American Society of Anesthesiologists (ASA) physical status classification of Class II or Class III; body mass index (BMI) between 18.5 and 30.0 kg/m²; no serious heart and lung diseases affecting surgery and anesthesia; no significant abnormalities in liver or kidney function; preoperative summary mental status examination (MMSE) score =26, There were no serious heart, brain, lung or other important organ diseases affecting surgery and anesthesia, and no obvious abnormality in liver and kidney functions; the score of preoperative MMSE was =26.

Exclusion criteria

Exclusion criteria: Allergy to the anesthetics used in the study; severe cardiac, hepatic, pulmonary, or renal insufficiency; preoperative cognitive dysfunction (MMSE score <26) or psychiatric disorders; long-term opioid treatment; pregnant or lactating females; patients weighing less than 40 kg or more than 100 kg; patients on lithium therapy or with contraindications to the use of the LiDCO system, such as puncture, or other conditions not suitable for participation in the study. Patients with severe peripheral vascular disease or anatomical changes at the puncture site, localized skin and soft tissue infections, severe coagulation disorders, or other conditions that make participation in this study inappropriate.

Design outcomes

Primary

MeasureTime frame
Postoperative cognitive function;

Countries

China

Contacts

Public ContactHuangZeQing

Liaoning Cancer Hospital & Institute

huangzeqing1973@163.com+86 189 0091 7545

Outcome results

None listed

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