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Observation on the Application Effect of Remazolam in Clinical Anesthesia

Observation on the Application Effect of Remazolam in Clinical Anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095223
Enrollment
Unknown
Registered
2025-01-03
Start date
2023-07-21
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Rectal cancer, endometrial cancer, cervical cancer, and prostate cancer, among others

Interventions

Experimental group:Remazolam was continuously pumped by 1mg/kg/h for anesthesia maintenance

Sponsors

The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age> 18 years old; 2.ASAI.~II; 3. Patients who intend to undergo lower abdominal and pelvic surgery under general anesthesia; 4.BMI >18kg/m2; 5. Patients or family members have a full understanding of the purpose and significance of this study, voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to the drug in this test 2. Patients with a history of cerebrovascular disease and preoperative intracranial hypertension; 3. Those with eye diseases and a history of eye surgery; 4. Patients with psychiatric diseases (such as schizophrenia, depression, etc.), history of epilepsy and cognitive dysfunction; 5. Those with a history of abuse of psychotropic drugs and narcotics in the past; 6. Suffering from severe vision or hearing disorders, unable to communicate smoothly, or illiterate; 7. ASA grade III or above, such as those with uncontrolled systemic diseases such as hypertension, diabetes, hyperthyroidism, patients with severe cardiopulmonary diseases, abnormal liver function, renal function, coagulation function, etc.; 8. Participated in other drug clinical trials as a subject in the past 3 months; 9. Subjects who, in the opinion of the investigator, have any other factors that are not suitable for participating in this trial.

Design outcomes

Primary

MeasureTime frame
Optic nerve sheath diameter;Mean blood flow velocity of the middle cerebral artery;Middle cerebral artery pulsatility index;Middle cerebral artery resistance index;

Countries

China

Contacts

Public ContactLu Xihua

Affiliated Cancer Hospital of Zhengzhou University (Henan Provincial Cancer Hospital)

hnlxh66@163.com+86 199 3767 0175

Outcome results

None listed

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