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Efficacy of remimazolam besylate versus propofol on hemodynamics during hysteroscopy: a randomized controlled trail

Efficacy and safety of remimazolam besylate versus propofol during hysteroscopy: a randomized controlled trail

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064828
Enrollment
Unknown
Registered
2022-10-19
Start date
2022-10-25
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

hypotension

Interventions

Group 1:General anesthetics
Group 2:Propofol

Sponsors

Shanghai First Maternity and Infant Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Women who plan to undergo hysteroscopic surgery; Aged 18-55 years; Body mass index (BMI) 18.5-30 kg/m^2; 2. American Society of Anesthesiologists (ASA) grade ? to ?.

Exclusion criteria

Exclusion criteria: 1. Patients who refused to participate in the trial; 2. Patients with acute upper respiratory tract infection, asthma attack and persistent state; 3. Severe cardiopulmonary disease; 4. Preoperative blood pressure of the day was > 160/100mmHg, or <90/60mmHg for patients with hypotension; 5. Patients with pathological obesity or OSAS; 6. Abuse of narcotic analgesics or sedatives; 7. Known allergy to general anesthesia; 8. Unable to communicate effectively and uncooperative.

Design outcomes

Primary

MeasureTime frame
Blood pressure;

Secondary

MeasureTime frame
Heart rate;Time between anesthesia induction and disappearance of eyelash reflex;The operation time;Anesthesia recovery time;Sedation scores;Drug use;Patients' satisfaction score;

Countries

China

Contacts

Public ContactLiu Zhiqiang

Shanghai First Maternity and Infant Hospital

drliuzhiqiang@163.com+86 21 20261000

Outcome results

None listed

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