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Determination of Effective Doses of Ciprofol–Esketamine and Propofol–Esketamine Combinations for Painless Gastroscopy:A Randomized, Double-Blind, Dose–Response Study

Determination of Effective Doses of Ciprofol–Esketamine and Propofol–Esketamine Combinations for Painless Gastroscopy:A Randomized, Double-Blind, Dose–Response Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125988
Enrollment
Unknown
Registered
2026-06-02
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

None

Interventions

Ciprofol 0.2mg/kg group:0.2mg/kg ciprofol combined with low-dose esketamine
Ciprofol 0.3mg/kg group:0.3mg/kg ciprofol combined with low-dose esketamine
Ciprofol 0.4mg/kg group:0.4mg/kg ciprofol combined with low-dose esketamine
Ciprofol 0.5mg/kg group:0.5mg/kg ciprofol combined with low-dose esketamine
Ciprofol 0.6mg/kg group:0.6mg/kg ciprofol combined with low-dose esketamine
Propofol 1.0mg/kg group:1.0mg/kg propofol combined with low-dose esketamine
Propofol 1.4mg/kg group:1.4mg/kg propofol combined with low-dose esketamine
Propofol 1.8mg/kg group:1.8mg/kg propofol combined with low-dose esketamine
Propofol 2.2mg/kg group:2.2mg/kg propofol combined with low-dose esketamine
Propofol 2.6mg/kg group:2.6mg/kg propofol combined with low-dose esketamine

Sponsors

Wenling First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I - III 2. BMI 18 - 28 kg/m² 3. No contraindications for gastroscopy 4. Age 18 - 64 years old

Exclusion criteria

Exclusion criteria: 1. The patient refuses to participate; 2. Allergic to esketamine, propofol or propofol; 3. Patients with severe risks of hypertension, hyperthyroidism, elevated intraocular pressure or intracranial pressure; 4. With a history of severe respiratory and cardiovascular diseases; 5. Currently taking opioid drugs and non-steroidal anti-inflammatory drugs; 6. With neurological disorders or mental disorders or having previous cognitive impairment; 7. Patients with impaired liver and kidney functions; 8. Pregnant or lactating women; 9. ASA classification of grade IV or V.

Design outcomes

Primary

MeasureTime frame
The number of effective and ineffective cases for each dose of ciprofol and propofol;The 50% effective dose (ED50) of ciprofol or propofol;

Secondary

MeasureTime frame
Gastroscopy examination time;The number of cases of artificial assisted breathing;Anesthesia recovery time;Vital signs after anesthesia induction with ciprofol and propofol;Mental symptoms related to esketamine;The number of additional cases of cyclopofol or propofol;

Countries

China

Contacts

Public ContactKang Lin

Wenling First People's Hospital

linkang66009@163.com+86 137 5866 0853

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026