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Comparative study on the sedative effect of ketamine, magnesium sulfate and propofol in endoscopy

Comparative study on the sedative effect of ketamine, magnesium sulfate and propofol in upper endoscopy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161205031252N12
Enrollment
201
Registered
2020-02-06
Start date
2020-01-17
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Condition 1: Diseases of upper digestive system which need endoscopy. Condition 2: Diseases of upper digestive system which need endoscopy. Gastric ulcer Barrett's esophagus

Interventions

Intervention 1: Control group: Amp midazolam,Daroopakhsh, 0.03 mg/kg, once, intravenous, before endoscopy + Amp propofol, Daroopakhsh, 1 mg/kg, once, intravenous, before endoscopy. Intervention 2: Int

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients aged more than 12 years

Exclusion criteria

Exclusion criteria: History of allergy to medications ASA physical status classification system more than 3

Design outcomes

Primary

MeasureTime frame
Physician's satisfaction of the adequacy of sedation for performing endoscopy. Timepoint: Immediately after completing the endoscopy. Method of measurement: Comfort score.;Patient's satisfaction of the adequacy of sedation for performing endoscopy. Timepoint: Immediately after completing the endoscopy. Method of measurement: Comfort score.;Sedation response score. Timepoint: Immediately after completing the endoscopy. Method of measurement: Ramsay sedation scale.

Secondary

MeasureTime frame
Recovery time. Timepoint: At the time of leaving recovery. Method of measurement: Time recording.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Hormati

Ghoum University of Medical Sciences

Hormatia@muq.ac.ir+98 25 3612 2053

Outcome results

None listed

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