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Effect of propofol combined with dezocine on patients undergoing indolent both gastroscopy and colonoscopy

Effect of propofol combined with dezocine on patients undergoing indolent both gastroscopy and colonoscopy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017630
Enrollment
Unknown
Registered
2018-08-07
Start date
2018-09-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

patients undergoing indolent both gastroscopy and colonoscopy

Interventions

Sponsors

Department of Anaesthesiology, The Fourth Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: ASA I–II level patients aged 18–85 years and scheduled for gastroscopy and colonoscopy will be included.

Exclusion criteria

Exclusion criteria: BMI>30 kg/m2; pre-existent circulation, respiratory and nervous systemic diseases; hemoglobin <70g/L; albumin< 30 g/L.

Design outcomes

Primary

MeasureTime frame
oxygen saturation;blood pressure;induction time;the induction dosage of propofol;the incidence and degree of reflex coughing and gagging;incidence of body movement;incidence of respiratory depression;the use of jaw thrust;incidence of assisted ventilation;incidence of using vasoactive drugs;duration of procedure;Steward score;the total dosage of propofol;awake time;the patient’s pain score;

Countries

China

Contacts

Public ContactZhang Limin

Department of Anaesthesiology, The Fourth Affiliated Hospital of Harbin Medical University

chizhang75@163.com+86 13115501086

Outcome results

None listed

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