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The Effects of Fospropofol disodium and Propofol on Hemodynamic Changes and Postoperative Cognitive Dysfunction during General Anesthesia Induction for Laparoscopic Colorectal Cancer Surgery in the Elderly: A Randomized Controlled Study

The Effects of Fospropofol disodium and Propofol on Hemodynamic Changes and Postoperative Cognitive Dysfunction during General Anesthesia Induction for Laparoscopic Colorectal Cancer Surgery in the Elderly: A Randomized Controlled Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100980
Enrollment
Unknown
Registered
2025-04-17
Start date
2025-03-21
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Postoperative pain after colorectal cancer surgery

Interventions

The group of Fospropofol disodium (Group F):Sufentanil 0.3 µg/kg was intravenously injected, and propofol disodium phosphate was diluted to 20 ml at a concentration of 10 mg/kg for intravenous infusi
Propofol group (Group P):Sufentanil was administered intravenously at a dose of 0.3 µg/kg, and propofol was diluted to 20 ml by a concentration of 2 mg/kg for intravenous infusion.

Sponsors

The Affiated Cancer Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 65 years old, gender not limited; 2.Scheduled for elective laparoscopic radical resection of colorectal cancer; 3.ASA classification II-III; 4 Preoperative Mini-Mental State Examination (MMSE) score >= 24 points; 5.Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1.Severe cardiovascular and cerebrovascular diseases (such as NYHA classification >= III grade or LVEF = 160/100 mmHg); acute coronary syndrome or stroke occurred within 6 months); 2.Abnormal liver and kidney functions (ALT/AST > 2 times upper limit, eGFR 7.5%); 4.Long-term use of sedatives/anxiolytic drugs before surgery (> 1 month); 5.History of dementia or mental illness; 6.Allergy to propofol or soybean/eggs; 7.More than 1 intubation or intubation time > 30 seconds; 8.Surgery time 4 hours, intraoperative blood loss > 15 ml/kg or intraoperative blood transfusion; 9.Postoperative admission to ICU.

Design outcomes

Primary

MeasureTime frame
Cardiovascular hemodynamic indicators at each time point during the induction period;Montreal Cognitive Assessment Scale MoCA-Basic;Confusion Assessment Method Scale;The incidence of hypotension during general anesthesia induction;

Secondary

MeasureTime frame
Time of awakening and occurrence of postoperative complications;

Countries

China

Contacts

Public ContactWan Qing

The Affiliated Cancer Hospital of Guizhou Medical University

34219463@qq.com+86 189 8438 5627

Outcome results

None listed

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