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Comparison the sedation effect and satisfaction of two combination ??(Dexmedetomidine and fentanyl with Midazolam and fetanyl)in patients ?undergoing bronchoscopy?

Comparison the sedation effect and satisfaction of two combination ??(Dexmedetomidine and fentanyl with Midazolam and fetanyl)in patients ?undergoing bronchoscopy?

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141209020258N76
Enrollment
92
Registered
2018-05-16
Start date
2018-01-14
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

sedation. Failed moderate sedation during procedure

Interventions

Intervention 1: Intervention group: We inject 30 micro gram dexmedetomidin (hospira)in first group. Intervention 2: Intervention group: We inject 3 milligram dexmedetomidin (Caspian)in second group.

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 18 to 70 years body mass index less than 30 Lack of sedation or anxiety or history of substance abuse No history of heart disease Insensitivity to Midazolam or egg or soy

Exclusion criteria

Exclusion criteria: pregnancy renal failure Neurological disorders tachicardia The percentage of oxygen saturation in the room air is higher than 90% of the initial state

Design outcomes

Primary

MeasureTime frame
Sedation ?. Timepoint: 5,10,15 and 20 minute after start of broncoscopy. Method of measurement: Ramsay score.;Heart rate. Timepoint: 5 and 15 minute after start of broncoscopy. Method of measurement: beat in minute.;Blood pressure. Timepoint: 5 and 15 minute after start of broncoscopy. Method of measurement: barometer.;Oxygen saturation. Timepoint: 5 and 15 minute after start of broncoscopy. Method of measurement: percent.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alireza Kamali

Arak University of Medical Sciences

alikamaliir@yahoo.com+98 86 3222 2003

Outcome results

None listed

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