Skip to content

Effect of neostigmine/glycopyrrolate versus sugammadex on postoperative delirium in elderly patients undergoing major noncardiac surgery: a randomized controlled trial

Effect of neostigmine/glycopyrrolate versus sugammadex on postoperative delirium in elderly patients undergoing major noncardiac surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093158
Enrollment
Unknown
Registered
2024-11-29
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Postoperative delirium

Interventions

Neostigmine/glycopyrrolate:Neostigmine + glycopyrrolate

Sponsors

The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age = 65 years old, male or female; 2) ASA grades I-III; 3) Undergoing major non-cardiac and non-neurosurgical procedures (thoracic, abdominal, urologic, orthopedic, and spine surgery) with an estimated surgical time = 1.5 hours; 4) Estimated discharge from the PACU to surgical wards after surgery and postoperative hospital stay = 2 days; 5) A clear understanding of the study and providing a written informed consent.

Exclusion criteria

Exclusion criteria: 1) Allergy to the drugs in the study; 2) Neostigmine contraindications (epilepsy, intestinal obstruction, urinary tract obstruction, asthma, glaucoma), paralysis, or neuromuscular diseases; 3) Severe liver insufficiency (Chil-Pugh grade C) or renal failure; 4) Long-term use of cholinesterase inhibitors, anticholinergic drugs or psychotropic drugs; 5) Inability to communicate effectively or refusal to participate in research.

Design outcomes

Primary

MeasureTime frame
Incidence of POD;

Secondary

MeasureTime frame
Days with POD and percentage in postoperative hospital stay;Postoperative cognitive function;Peak CAM-S score and sum of CAM-S scores;

Countries

China

Contacts

Public ContactPeng Ke

Department of Anesthesiology, The First Affiliated Hospital of Soochow University

pengke@suda.edu.cn+86 159 6215 5989

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 2, 2026