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"Comparison of the effect of Dexmedetomidine + Marcaine with Fentanyl + Marcaine in femur fracture surgery"

Comparison of the analgesia effect of Dexmedetomidine with Fentanyl, in combination with Marcaine in femoral neck fracture surgery with spinal anesthesia

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230805059046N1
Enrollment
75
Registered
2023-09-03
Start date
2023-08-23
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Femoral neck fracture surgery. Fracture of head and neck of femur

Interventions

Intervention 1: Intervention group A: (25 µg/kg Fentanyl from Caspian Tamin Pharmaceutical Company and 2.5 mg/kg Marcaine from Adorateb Pharmaceutical Company). After patients enter the operating room

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in research with informed consent after giving necessary and sufficient explanations about the study The person's age should be between 45 and 75 years No history of surgery No history of smoking, alcohol and drugs Not having chronic physical or mental illness (schizophrenia, diabetes, etc.) Not having vision and hearing problems and other disabilities Not using corticosteroids, antihistamines, narcotics and painkillers for a long time Lack of allergy to marcaine, fentanyl and dexmedomidine Absence of pregnancy, breastfeeding and abortion less than 3 months

Exclusion criteria

Exclusion criteria: Unwillingness to cooperate in the study Occurrence of any problems and complications during the study The diagnosis of the surgeon or other specialists to withdraw from the study Heart diseases and HTN Liver diseases (cirrhosis, hepatitis, etc.)

Design outcomes

Primary

MeasureTime frame
The amount and intensity of pain. Timepoint: 3, 6 and 12 hours after the operation. Method of measurement: Using a ruler-like grading system (Visual Analog Scale) from 0 (no pain) to 10 (the most severe pain imaginable).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParia Talebnezhad

Qazvin University of Medical Sciences

Paria.Talebnezhad8898@gmail.com+98 28 3333 6001

Outcome results

None listed

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