Comparison of the effect of intravenous and spinal dexmedetomidine on the quality of spinal anesthesia in patients with inguinal hernia
- Conditions
- inguinal hernia.Inguinal hernia
- Registration Number
- IRCT20171030037093N23
- Lead Sponsor
- Bandare-abbas University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Patients 18 to 70 years old
Patient with ASA I, II undergo inguinal hernia surgery
Patients with ASA greater than or equal to III
spinal anesthesia contraindication (Coagulation problems, increased ICP, sepsis, infection)
Patients with potential sensitivity to anesthetic or dexmedetomidine
Patient with underlying neurological defect
Patients with addiction or with a history of chronic drug abuse or analgesia
Patients with heart block or unstable cardiovascular status
Patients receiving steroids and agonists
Patients with liver, kidney problems, adrenal and neuromuscular disorders, and diabetic patients
Patients with blockage failure who require medication or induction of general anesthesia.
Patients receiving agonist a2
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of pain. Timepoint: After surgery. Method of measurement: According to VAS.;Maximum level of sensory block. Timepoint: During surgery every ten minutes. Method of measurement: Through the cold feeling of cotton alcohol.;Block initiation rate up to T10. Timepoint: Once before surgery. Method of measurement: observation.;Sensory block recovery. Timepoint: Once after surgery. Method of measurement: observation.;Maximum level of motion block. Timepoint: During surgery every ten minutes. Method of measurement: Computing.
- Secondary Outcome Measures
Name Time Method