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Application of different doses of alfentanil combined with propofol in painless colonoscopy in elderly patients: a prospective, randomized controlled trial

Application of different doses of alfentanil combined with propofol in painless colonoscopy in elderly patients: a prospective, randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049166
Enrollment
Unknown
Registered
2021-07-24
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Painless Colonoscopy

Interventions

Experimental group1:2.5µg/kg alfentanil combined with 2mg/ml propofol
Experimental group2:5.0µg/kg alfentanil combined with 2mg/ml propofol
Experimental group3:7.5µg/kg alfentanil combined with 2mg/ml propofol
Experimental group4:10.0µg/kg alfentanil combined with 2mg/ml propofol

Sponsors

The Second Hospital of Jiaxing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with ASA I to III; 2. Aged 60 to 80 years; 3. Plan to undergo a painless colonoscopy (expected operation time < 30 minutes); 4. Body mass index 18.5-30 kg/m2.

Exclusion criteria

Exclusion criteria: 1. Patients without written consent; 2. ASAIV level or above; 3. Serious heart disease; 4. Lung disease; 5. Advanced or decompensated liver or kidney disease; 6. Metabolic diseases; 7. Electrolyte disorders; 8. Blood pressure > 180/110mmHg; 9. Allergy to emulsions or opioids; 10. A history of acute airway inflammation, neuromuscular or neuropsychiatric disorders, suspected abuse of narcotic analgesics or sedatives within the previous 2 weeks; 11. Exclude patients with difficult airway management, such as nail-mind spacing <=4cm or Mallampati score of 3 or 4.

Design outcomes

Primary

MeasureTime frame
Oxygen saturation reduction events [defined as peripheral capillary oxygen saturation below 95% and 90%];

Secondary

MeasureTime frame
Hemodynamic stability;Total consumption of propofol ;Operation time;Postanesthesia care unit retention time;pain score 1 minute after waking up ;Satisfaction of endoscopists, satisfaction of patients ;

Countries

China

Contacts

Public ContactXu Hai

The Second Hospital of Jiaxing

xuhai@jxey.com+86 15988375602

Outcome results

None listed

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