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Sedative effect of Remifentanil in Senile Cataract Surgeries

Comparison of the sedative effect of Remifentanil and Propofol in Senile Cataract Surgeries under Regional Block

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201111268201N1
Enrollment
60
Registered
2012-04-14
Start date
2010-12-22
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

Cataract. Senile incipient cataract

Interventions

Intervention 1: Control group: with bolus doses of 0.25 µg/kg and maintenance dose of 25 µg/kg/min. Intervention 2: Intervention group: with bolus doses of 0.5 µg/kg, and maintenance dose of 0.05 µg/k
Treatment - Drugs
Control group: with bolus doses of 0.25 µg/kg and maintenance dose of 25 µg/kg/min
Intervention group: with bolus doses of 0.5 µg/kg, and maintenance dose of 0.05 µg/kg/min

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ASA physical status 2,3; Male or female age=65 ; No Allergic Reaction to Drug; No Drug abuse; No smoking. Exclusion criteria: hypoxia; nausea; vomiting.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
O2 saturation. Timepoint: During intravenous sedation. Method of measurement: Pulseoximeter.;Sedation score. Timepoint: Before regional block and every 10 minutes therafter until the end of operation. Method of measurement: MOAA/SS (Modified observer's assessment of alertness/sedation).;Blood pressure. Timepoint: During intravenous sedation. Method of measurement: By non-invasive blood pressure measuring.;Heart rate. Timepoint: During intravenus sedation. Method of measurement: ECG.

Secondary

MeasureTime frame
Nausea and vomiting. Timepoint: During intravenous sedation. Method of measurement: Observe.;Bradycardia. Timepoint: during intravenous sedation. Method of measurement: Electrocardiogram (ECG).;Apnea. Timepoint: during intravenous sedation. Method of measurement: Respiratoty Rate.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Tarjoman Porshokoh

Tehran University of Medical Sciences

r_tarjoman@yahoo.com+98 21 8833 3556

Outcome results

None listed

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