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Comparison between sedation with subcutaneuos ketamine and sedation with propofol in patients undergoing colonoscopy procedures

Comparison between dissociative conscious sedation and sedation with propofol in patients undergoing colonoscopy procedures

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205079660N1
Enrollment
48
Registered
2012-09-29
Start date
2012-09-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Mental and behavioural disorders due to use of sedatives or hypnotics. Mental and behavioural disorders due to use of sedatives or hypnotics

Interventions

Intervention 1: First group will receive 2microgram/kg fentanyl + propofol 50-75 mg/kg during the procedure and if needed additional fentanyl will be added up to 4 micro/kg. Intervention 2: The second
Treatment - Drugs
First group will receive 2microgram/kg fentanyl + propofol 50-75 mg/kg during the procedure and if needed additional fentanyl will be added up to 4 micro/kg.
The second group will receive 2microgram/kg fentanyl + 0.6 mg/kg SQ ketamine during the procedure and if needed additional fentanyl up to 4 micro/kg will be added. The site of SQ injection is in fron

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patients in ASA class 1 or 2 (without underlying disease or with mild underlying disease which is well controlled by medication) undergoing colonoscopy; age between 18-60. Exclusion criteria: any uncontrolled or poor controlled underlying disease; seizure disorders; history of hypersensitivity to egg or any drug; addiction to narcotics; mental retardation or any cognitive disorder.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
SPO2. Timepoint: Continuous. Method of measurement: pulse oxiometery.;Blood pressure. Timepoint: every 5 minutes. Method of measurement: noninvasive cuff measurrment.;Heart rate. Timepoint: every 5 minutes. Method of measurement: pulse counting.

Secondary

MeasureTime frame
Apnea. Timepoint: continuous. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSanaz Sha`bani

Tehran University of Medical Sciences

sanazshaabani@yahoo.com+98 21 61190

Outcome results

None listed

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