Skip to content

Half effective dose of remimazolam toluenesulfonic acid combined with sufentanil to inhibit laryngeal mask placement in patients undergoing hysteroscopic electrotomy: a double-blind, prospective study

Half effective dose of remimazolam toluenesulfonic acid combined with sufentanil to inhibit laryngeal mask placement in patients undergoing hysteroscopic electrotomy: a double-blind, prospective study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079790
Enrollment
Unknown
Registered
2024-01-12
Start date
2024-01-15
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

None

Interventions

High-dose sufentanil group:Sufentanil 0.35ug/kg
Low dose sufentanil group:Sufentanil 0.25ug/kg

Sponsors

Nanchong Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who underwent daytime hysteroscopic resection were aged between 18 and 65 years. 2. Body mass index 18-28kg/m^2; 3. ASAI - Class II; 4. Patients who agree to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. A history of diseases of the nervous, muscular and endocrine systems; Serious organic diseases, such as serious heart, lung, liver, kidney, brain and other disorders; 2. Poorly controlled hypertension such as systolic blood pressure =180mmHg or diastolic blood pressure =110mmHg; 3. Acute respiratory infections, COPD, and poorly controlled asthma 4. A history of long-term use of neuropsychiatric drugs such as antidepressants and anti-anxiety drugs or a history of benzodiazepines in the past three months; Cardiac hand Surgical history, cerebrovascular accident history, alcoholism history; 5. People who are allergic to the study drug; 6. Patients with expected difficult airway; 7. Pregnant and lactating women; 8. There are social psychological problems and other reasons can not cooperate.

Design outcomes

Primary

MeasureTime frame
Median effective dose of Remimazolam;

Secondary

MeasureTime frame
Remazolam 95% effective dose;Patients' vital signs (SBP,DBP,MAP, HR, SPO2) at various time points during anesthesia induction;Number of adverse reactions during induction and within 5 minutes after laryngeal mask placement (hypotension, bradycardia, hypoxemia, injection pain, etc.);Number of postoperative adverse reactions (intraoperative awareness, postoperative nausea and vomiting, etc.);Demographic indicators (such as age, weight, height, etc.);

Countries

China

Contacts

Public ContactXie Ying

Nanchong Central Hospital

475153895@qq.com+86 181 8017 4206

Outcome results

None listed

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