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Midazolam sedation in endoscopy

Intranazal midazolam efficacy in upper endoscopy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110087740N1
Enrollment
105
Registered
2013-04-22
Start date
2010-10-10
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

Upper endoscopy. Upper endoscopy for evaluation of upper GI diseases

Interventions

Intranazal midazolam 1mg in intervention group and pure water in control..
Treatment - Drugs
Intranazal midazolam 1mg in intervention group and pure water in control.

Sponsors

Ahvaz University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criterion: patients aged between 20 to 60 years old candidate for upper endoscopy. Exclusion criteria:GIB; COPD; CHF and intolerance to upper endoscopy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Midazolam sedation for making upper endoscopy more comfort. Timepoint: 2 hours after intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Amnesia after endoscopy. Timepoint: 2 hours after endoscoy. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHajiani Eskandar

Ahvaz University of Medical Sciences and Health Services

eskandarhajiani@yahoo.com+98 611222292

Outcome results

None listed

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