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Clinical Observation of Remimazolam Combined with Alfentanil in Outpatient Painless Colonoscopy

Clinical Observation of Remimazolam Combined with Alfentanil in Outpatient Painless Colonoscopy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053470
Enrollment
Unknown
Registered
2021-11-22
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-10-04

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

Conditions

Painless Colonoscopy

Interventions

Propofol group:5ug/kg of alfentanil and propofol (1.5mg/kg)
Remazolam group:5ug/kg of alfentanil and remimazolam (1.5mg/kg)

Sponsors

Weifang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients receiving painless colonoscopy diagnosis and treatment; 2. Aged 18-65 years, gender is not limited; 3. ASA I-II grade; 4. BMI 18-30kg/m^2; 5. Informed consent, voluntarily participate in the trial, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, brain, lung, liver, kidney and metabolic diseases; 2. Systolic blood pressure > 180mmHg and (or) diastolic blood pressure > 110mmHg in patients with preoperative blood pressure, or 40%/150ml of wine); 6. Those who are allergic to or have contraindications to aniline azepines, opioids, propofol, lidocaine and their drug components; 7. Subjects deemed unsuitable by the investigator to participate in this study.

Design outcomes

Primary

MeasureTime frame
Intraoperative adverse events occurred ;

Secondary

MeasureTime frame
Effectiveness index;vital signs;Safety index;Satisfaction evaluation ;

Countries

China

Contacts

Public ContactCheng Xiaoyan

Weifang People's Hospital

chxy13608951177@qq.com+86 13608951177

Outcome results

None listed

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