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Effect of Remazolam on Anesthesia Recovery in Patients Undergoing Fundus Surgery

Effect of Remazolam on Anesthesia Recovery in Patients Undergoing Fundus Surgery-A Single-center, Prospective, Randomized, Double-blind, Controlled Clinical Trial

Status
Not yet recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06205719
Enrollment
93
Registered
2024-01-16
Start date
2024-06-01
Completion date
2026-05-30
Last updated
2024-05-20

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

Conditions

Postoperative Recovery, Remazolam Anesthesia

Brief summary

to investigate the effect of remazolam benzenesulfonate in patients with ocular fundus surgery, so as to guide clinical anesthesiologists to choose more appropriate anesthetic drugs in fundus surgery

Detailed description

to investigate the effect of remazolam benzenesulfonate in patients with ocular fundus surgery, so as to guide clinical anesthesiologists to choose more appropriate anesthetic drugs in fundus surgery。There are three groups.In Group H, ciprofol + Remifentanil was used for maintenance of anesthesia, in Group R, remifentanil + Remifentanil was used for maintenance of anesthesia, in Group RF, remifentanil + Remifentanil was used for maintenance of anesthesia, at the end of the operation, flumazenil was used to counteract the residual anesthetic effect.The quality of postoperative recovery was compared

Interventions

DRUGciprofol

sedation

sedation

DRUGFlumazenil

antagonism

DRUGRemifentanil

2ug/kg Remifentanil

Sponsors

Sichuan Provincial People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. ASA I-II, patients 2. aged 18-65 years old; 3. Fundus surgery to be performed under general anesthesia ; 4. The expected duration of surgery is about 30-120 min ; 5. BMI: 18-30 kg/m2 ; 6. Those who signed the informed consent form and volunteered to participate in this trial

Exclusion criteria

1. Patients with known or suspected genetic susceptibility to malignant hyperthermia; 2. Patients with history of asthma; 3. Patients with severe heart diseases (NYHA ≥ III, severe arrhythmia, etc.) and cerebral or pulmonary diseases, liver or kidney dysfunction; or with unstable vital signs; 4. Patients with history of long-term narcotic analgesics application, including sedative and antidepressant drugs; 5. Patients with history of psychotropic drug abuse within 3 months; 6. Patients with long-term alcohol abuse; 7. People with mental disorder and unable to communicate normally;

Design outcomes

Primary

MeasureTime frameDescription
time for recovery3 second to 30minutesThe time from stopping the anesthetic to waking up

Contacts

Primary ContactYanYu Liu
43197113@qq.com13438348895

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026