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The effect of intravenous infusion of remifentanil and dexmedetomidine on hemodynamic changes and pain in patients undergoing cataract surgery

The effect of intravenous infusion of remifentanil and dexmedetomidine on hemodynamic changes and pain in patients undergoing cataract surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220302054164N2
Enrollment
122
Registered
2023-01-19
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Cataract. Age-related cataract

Interventions

Intervention 1: Intervention group: Dexmedetomidine recipient Receiving ./5 µg/kg/h of dexmedetomidine from Elixir company using an infusion pump from the onset of induction of anesthesia to the end o

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 75 Years

Inclusion criteria

Inclusion criteria: All patients referred to Amirkabir Arak Hospital for cataract surgery signing informed consent by patients Patients age 25-75 years American Society of Anesthesiologists (ASA) physical status classification I & II Candidates of local anesthesia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hemodynamic variables based on the questionnaire. Timepoint: During surgery and recovery. Method of measurement: monitoring devices.;Emergence agitation. Timepoint: Recovery room. Method of measurement: Richmond Agitation and Sedation Scale (RASS).;Pain score. Timepoint: recovery. Method of measurement: The Visual Analogue Scale (VAS).;Surgeon satisfaction. Timepoint: During surgery. Method of measurement: Asking the surgeon.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSafoora Omidvar

Arak University of Medical Sciences

s_omidvar1991@yahoo.com+98 86 3417 3526

Outcome results

None listed

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