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Effects of age on Optimal effect-site concentration of remimazolam for efficacy of general anesthetic duction in female patients

Effects of age on Optimal effect-site concentration of remimazolam for efficacy of general anesthetic duction in female patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0008120
Enrollment
90
Registered
2023-01-13
Start date
2023-01-09
Completion date
Unknown
Last updated
2023-02-08

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

Conditions

None listed

Interventions

Drug : In order to induce general anesthesia, inject Remimazolam prepared at a concentration of 1 mg/ml as a bolus through a syringe pump at a dose calculated in advance for about 1 minute. If the

Sponsors

Ajou University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Female patients (20-39 years old group, 40-59 years old group, 60-75 years old group ) who correspond to ASA 1 and 2, weight <100 kg, and are scheduled to general anesthesia.

Exclusion criteria

Exclusion criteria: Patients with BMI > 30 kg/m2 or < 20 kg/m2, patients with contraindications such as allergies to this study drug, patients with hearing impairment, etc., who are unable to respond to the researcher's verbal command, or patients with liver disease (bilirubin =3.0 mg/dl, or aspartate amino transferase/alanine aminotransferase = 2.5 x upper limits of normal), renal disease (creatine = 2 mg/dl), chronic obstructive pulmonary disease, uncontrolled hypertension ( e.g. Patients with systolic BP =160 mmHg), diabetes (HbA1c = 9%), moderate to severe coronary artery disease, glaucoma, heart failure, or taking other medications that may affect the effectiveness of benzodiazepines despite taking blood pressure medications If present, a history of smoking (within the last 6 months). If the IV line is placed on the back of the hand.

Design outcomes

Primary

MeasureTime frame
Differences in EC50 and EC95 for anesthesia induction effect in each group

Secondary

MeasureTime frame
Check loss of consciousness (LOC) every 10 seconds for 90 seconds after drug administration;Difference in time to LOC in each group;Differences in the occurrence of postoperative nausea and vomiting (PONV) and the degree of pain in each group of patients

Countries

Korea, Republic of

Contacts

Public ContactEunji Ha

Ajou University Hospital

111791@aumc.ac.kr+82-31-219-4658

Outcome results

None listed

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