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A study of the effect of short-term inhalation of xenon during anesthesia for prevention of postoperative delirium in elderly patients undergoing laparoscopic radical colectomy

A study of the effect of short-term inhalation of xenon during anesthesia for prevention of postoperative delirium in elderly patients undergoing laparoscopic radical colectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076666
Enrollment
Unknown
Registered
2023-10-16
Start date
2023-11-20
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Postoperative Delirium (POD), Colorectal Cancer

Interventions

control subjects:Inhalation of 50% nitrogen and 50% oxygen
experimental group:Inhalation of 50% xenon/50% oxygen

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 65-80 years; 2.Patients undergoing elective laparoscopic colon cancer surgery; 3.American Society of Anesthesiologists (ASA) physical status I-III; 4.Ability to read and understand study materials and provide written informed consent.Only those who meet the above four criteria can be included in this study.

Exclusion criteria

Exclusion criteria: 1. History of allergy to xenon or anesthetic agents used during the study; 2. A history of psychiatric disorders such as depression, anxiety, schizophrenia, or mood disorders; 3. MMSE scores indicative of significant cognitive impairments (education level above secondary level 6 hours; 11. Concurrent participation in another clinical trial.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative delirium as assessed by 3-Minute Diagnostic Interview for Confusion Assessment Method 3D-CAM);

Secondary

MeasureTime frame
Severity of POD assessed with Delirium Rating Scale-Revised-98 (DRS-R-98) and the Confusion Assessment Method-Severity (CAM-S);POD onset time;duration of POD episode;POD subtypes, which were assessed using "Richmond Agitation-Sedation Scale";pain levels at rest and during movement, which were assessed daily by Visual Analogue Scale;sleep quality, which was determined daily by "Pittsburgh Sleep Quality Index";intraoperative hemodynamic and respiratory parameters;liver and kidney function, serum C-reactive protein level within postoperative 3 days, non-delirium complications throughout the observed period, and hospitalization costs;

Countries

China

Contacts

Public ContactJin Mu

Beijing Friendship Hospital, Capital Medical University

jinmu0119@hotmail.com+86 133 6660 0987

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026