Skip to content

Effect of remazolam versus propofol on retention and delayed regenerative memory before and after anesthesia

Effect of remazolam versus propofol on retention and delayed regenerative memory before and after anesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080979
Enrollment
Unknown
Registered
2024-02-20
Start date
2024-02-20
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Large cryptic varices

Interventions

RM group:no
PO group:no

Sponsors

Zhongshan Hospital(Xiamen), Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? Patients undergoing elective large saphenous vein surgery; ? Age is 18~65 years old, and gender is not limited; ? Body mass index (BMI): 18 ~ 28 kg/m2; ? American Association of Anesthesiologists' Classification (ASA): Grade I to II; ? The large saphenous vein operation lasts within 3h; ? The drug used is remazolam or propofol; The subjects voluntarily participated in the trial and signed the informed consent form for this trial.

Exclusion criteria

Exclusion criteria: ? The subject explicitly refused to participate in the study; ? Allergic to opioids, benzodiazepines, propofol, flumazenil, or naloxone drug excipients; ? Use ß blockers, anxiolytics and antidepressants; ? Suspected abuse of narcotic analgesics or sedatives, and alcoholics; ? Electrocardiogram suggests: heart rate 100 times / min or severe arrhythmia; ? History of acute respiratory infection within 2 weeks; ? Have a history of serious heart, brain, lung, liver, kidney or metabolic diseases, have neuromuscular system diseases (such as myasthenia gravis), mental diseases; ? Systolic blood pressure> 180 mmHg and (or) diastolic blood pressure> 110 mmHg in patients with preoperative hypertension, or <90 / 60 mmHg in patients with hypotension; ? History of thyroid or neck surgery; ? Previous history of abnormal surgical anesthesia recovery; ? To dict those who may or have difficult airway, such as modified horse grade-grade; ? Pregnancy or lactating women and patients with birth planning within 3 months (including men); ? Other subjects considered unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
Patient's picture recognition and recall before and after drug administration;

Secondary

MeasureTime frame
Anesthesia awakening time;The amount of the opioids used;The incidence of the observed postoperative adverse effects;

Countries

china

Contacts

Public ContactYuejiao Song

Zhongshan Hospital(Xiamen), Fudan University

15859252802@163.com+86 158 5925 2802

Outcome results

None listed

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