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Comparative study on the antianxiety effect of remimazolam besylate and ciprofol after hysteroscopy

Comparative study on the antianxiety effect of remimazolam besylate and ciprofol after hysteroscopy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073064
Enrollment
Unknown
Registered
2023-06-30
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Abnormal uterine bleeding

Interventions

Group Remimazolam(Group R):Remimazolam+Remifentanil
Group Ciprofol(Group C):Ciprofol+Remifentanil

Sponsors

Mengcheng County No. 1 People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria 1. Patients undergoing elective hysteroscopy; 2. Age 18-65 years old; 3. ASA is classified as Grade I-II; 4. BMI 18-30 kg/m2 5. Able to understand and complete the questionnaire with the assistance of medical staff; 6. Voluntarily participate in the trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Mental illness, Disorders of consciousness or inability to communicate; 2. Have a history of allergy to Narcotic and Contraindication of remiazolam and cyclopol; 3. Taking Antidepressant, Anxiolytic or other psychotropic drugs for a long time (more than 3 months); 4. Unable to understand or refuse to complete the questionnaire;

Design outcomes

Primary

MeasureTime frame
PAS-7;VAS-A;

Secondary

MeasureTime frame
Demography information and surgical information;Incidence of adverse reactions;

Countries

China

Contacts

Public ContactXiaoqiang Zhang

Mengcheng County No. 1 People’s Hospital

zxqahl@126.com+86 133 0967 0321

Outcome results

None listed

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