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The research of low-dose esketamine combined with propofol in colonoscopy

The research of low-dose esketamine combined with propofol in colonoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066052
Enrollment
Unknown
Registered
2022-11-22
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Digestive system diseases

Interventions

esketamine group:esketamine 0.15 mg/kg + propofol 1-1.5 mg/kg
saline group:0.9% NaCl 0.15 ml/kg + propofol 1-1.5 mg/kg

Sponsors

The First Affiliated Hostipal of Xi'an Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18 - 65 years; 2. ASA grade I-II; 3. Body mass index (BMI) 18-28 kg/m2; 4. Patient to undergo colonoscopy under sedation/anaesthesia; 5. Voluntary signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Psychiatric disorders (e.g. schizophrenia, depression, etc.); 2. Bradycardia (heart rate <= 50 beats/min) and severe arrhythmias; 3. Poorly controlled or untreated hypertension, diabetes mellitus, coronary artery disease; 4. Hyperthyroidism or hypothyroidism; 5. History of OSAHS or a combined difficult airway; 6. History of previous psychotropic and narcotic drug abuse; 7. History of abdominal surgery; 8. Pregnant or lactating women; 9. Allergy to experimental drugs.

Design outcomes

Primary

MeasureTime frame
consumption of propofol;

Secondary

MeasureTime frame
awakening time;sedation related adverse events;postanesthesia care unit dwell time;

Countries

China

Contacts

Public ContactHan Bin

The First Affiliated Hostipal of Xi'an Medical University

38598383@qq.com+86 185 9178 7502

Outcome results

None listed

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