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Comparison of the effect of Intrathecal addition of Dexmedetomidine and Sufentanil to Bupivacaine in Patients Undergoing Knee Prosthesis

Phase 3
Conditions
pain.
Pain, not elsewhere classified
Registration Number
IRCT20141001019359N12
Lead Sponsor
Bojnourd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
90
Inclusion Criteria

Be vigilant
Do not Have history of previous surgery,
Do not Have history of taking anti-anxiety, analgesic and sedative drugs
Do not Have history of allergies to drugs used in the study
Do not have drug addiction.
Age between 40 to 70 years

Exclusion Criteria

Patients undergoing general anesthesia for any reason after spinal anesthesia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
evel of analgesia. Timepoint: After performing spinal anesthesia technique. Method of measurement: Pin Prink method.;Duration of analgesia. Timepoint: The patient's first request for an analgesic injection. Method of measurement: Researcher-made questionnaire.;Intensity of pain. Timepoint: The patient's first request for an analgesic injection. Method of measurement: visual analog scale.
Secondary Outcome Measures
NameTimeMethod
Physiological parameters (blood pressure, heart rate, mean arterial pressure). Timepoint: After the spinal technique, for the first 15 minutes every 2 minutes and then every 4 minutes until the end of surgery. Method of measurement: Cardiac monitoring.;Drug side effects. Timepoint: End of surgery up to 24 hours later. Method of measurement: Researcher-made questionnaire.
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