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Application of remazolam in hysteroscopic surgery: a randomized controlled trial

Application of remazolam in hysteroscopic surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057034
Enrollment
Unknown
Registered
2022-02-26
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

Endometrial disease

Interventions

group 1:remazolam 0mg/kg
group 2:remazolam 0.1mg/kg
group 3:remazolam 0.15mg/kg
group 4:remazolam 0.2mg/kg
group 5:remazolam 0.25mg/kg
group 6:remazolam 0.3mg/kg

Sponsors

Women's Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing hysteroscopic surgery under intravenous anesthesia, ASA grade I-II, aged 20-50 years, BMI 18-24. 2. No electrolyte disorders, diseases of infection, immune system or endocrine system; no cardiovascular drugs, non-steroidal anti-inflammatory drugs, hormone drugs or antipsychotic drugs taken recently.

Exclusion criteria

Exclusion criteria: 1. Previous history of vaginal delivery; 2. Patients with abnormal liver and kidney function; 3. History of cardiopulmonary disease; 4. Sleep apnea syndrome; 5. Long-term use of drugs such as diazepam; 6. Chronic use of opioids; 7. Remazolam allergy.

Design outcomes

Primary

MeasureTime frame
Half effective concentration of propofol;

Secondary

MeasureTime frame
Intraoperative vital signs;The recovery time;

Countries

China

Contacts

Public ContactChen Xinzhong
chenxinz@zju.edu.cn+86 18806523402

Outcome results

None listed

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