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Sadation for colonoscopy: a double-blind comprison of ketamin and pethidine / midazolam combination

Sadation for colonoscopy: a double-blind comprison of ketamin and pethidine / midazolam combination

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015100324306N1
Enrollment
100
Registered
2015-11-03
Start date
2013-09-23
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

sedation. Other sedatives, hypnotics and antianxiety drugs

Interventions

Intervention 1: 0.5mg/kg ketamine, 15 min before colonoscopy subcutaneously. Intervention 2: 25mg pethidine plus 2.5 mg midazolam intravenously before the procedure.
Treatment - Drugs
0.5mg/kg ketamine, 15 min before colonoscopy subcutaneously
25mg pethidine plus 2.5 mg midazolam intravenously before the procedure

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: colonoscopy not in a emergency situation; patient satisfaction; lack of sensitivity to anesthetics; lack of mental retardation & cognitive impairment; no history of drug addiction; no anatomic abnormalities such as partial colectomy or colostomy or intestinal adhesions. Exclusion criteria: BP>140/90; psychosis; patient admission in psychiatric ward.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Analgesic effect. Timepoint: after colonoscopy. Method of measurement: pain scale.;Nausea and vomiting. Timepoint: after colonoscopy,two hours after colonoscopy. Method of measurement: check list.;Arterial oxygen saturation percentage. Timepoint: before the procedure,During the process. Method of measurement: pulse oximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Massoumi

Tehran University of Medical Sciences

s-massoumi@razi.tums.ac.ir; sara.2104@yahoo.com+98 21 8896 1696

Outcome results

None listed

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