A Comparison between the sedative effect of Fentanyl and Ketamine outside the operating room.
Phase 2
Recruiting
- Conditions
- Pain management of patients referred for Colonoscopy and reduce their anxiety.
- Registration Number
- IRCT20200818048445N1
- Lead Sponsor
- Ahvaz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 144
Inclusion Criteria
They are between 18 and 65 years old
Patients are referred for colonoscopy procedure
Classification of Group 1 and 2 American Society of Anesthesiologists (ASA Class I & II) are selected as inclusion criteria.
Exclusion Criteria
the patient's unwillingness to participate in the study
They are under 18 years old
They are over 65 years old
They have kidney failure
They have liver failure
They have chronic pain syndrome
They are addicted
They have any drug allergies
They have cardiovascular disease
They have a respiratory disease
They have metabolic diseases
They have a neurological disease
They have difficult airways
The patient is classified as ASA class 3 and 4
Contraindicated propofol ketamine or propofol fentanyl
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A score of 5 or 6 RAMSAY criteria in the questionnaire. RAMSAY sedation criteria including 6 scores is as follows: 1. Completely awake and anxious 2. Quiet and calm with enough cooperation 3. Asleep and wakes up with a verbal command 4. Asleep and woke up with mild stimulation, but gives a strong reaction to painful stimuli 5. Slow reaction to painful stimuli 6. Lack of reaction to painful stimuli. Timepoint: 5 minutes after the procedure, 10 minutes after the procedure, 15 minutes after the procedure. Method of measurement: Verbal measurement criteria.
- Secondary Outcome Measures
Name Time Method