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Effects of intravenous administration of remazolam on cognitive function, sleep quality and comfort in elderly patients after surgery

The effect of remazolam on cognitive function, sleep quality and comfort in elderly patients after surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041189
Enrollment
Unknown
Registered
2020-12-21
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-03-01

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

Conditions

Gastrointestinal disease

Interventions

Propofol group:Propofol intravenous induction and maintenance
remazolam group:Remazolam intravenous induction and maintenance

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 65-80 years, no gender limit; 2. Patients undergoing laparoscopic gastrointestinal surgery (such as radical resection of gastric and colorectal cancer, etc.) under general anesthesia; 3. ASA classification I-III; 4. 18kg/m2 <= BMI <= 30 kg/m2; 5. Able to understand the research process and the use of cognitive scales, and be able to communicate effectively with researchers; 6. Volunteer to participate and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who have participated in other drug clinical trials in the past 3 months; 2. Those with incomplete clinical examination data and those who think it is inappropriate to participate in this experiment; 3. People with communication disorders (language disorders, mental disorders); 4. People with cardiovascular diseases such as severe atrioventricular block and severe cardiac insufficiency; 5. People who are known to be intolerant or allergic to the experimental drugs used in this study; 6. Accompanied by peripheral vascular disease, sleep disorders, and recent use of antidepressants and hypnotics; 7. Have a history of neurological diseases: history of head injury, intracranial hypertension, cerebral aneurysm, cerebrovascular accident.

Design outcomes

Primary

MeasureTime frame
Ratio of Perioperative neurocognitive disorders;

Secondary

MeasureTime frame
nausea and vomiting;Sleep quality;Incidence of injection pain;Incidence of dizziness;Serum neuron injury factors level;Serum inflammatory factors level;Patient satisfaction score for anesthesia;

Countries

China

Contacts

Public ContactXia Zhongyuan

Renmin Hospital of Wuhan University

Xiazhongyuan2005@aliyun.com+86 027-88041911-81028

Outcome results

None listed

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