Dexmedetomidine in Sonographic Guided Erector Spinae Plane Block
- Registration Number
- NCT06899841
- Lead Sponsor
- Assiut University
- Brief Summary
to investigate the postoperative analgesic effect of dexmedetomidine addition with different doses as an adjuvant to bupivacaine to Erector spinae plane block after renal surgeries.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 90
- Age between 18 and 70 years.
- Both sexes, males and females.
- Patients with the American Society of Anesthesiologists (ASA) physical status I/II.
- Body mass index (BMI) of 18-35 kg/m2
- Patients scheduled for elective Renal or Percutaneous Nephrolithotomy.
- Patients under 18 years.
- Patient refusal of nerve block.
- Infection at the site of injection.
- Coagulopathy.
- Allergy to used medications.
- Psychiatric disorder or chronic pain syndromes.
- Chronic opioid use or substance abuse.
- Quadriplegic patients.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description low dose dex Dexmedetomidine 0.5 mic/kg of dexmedetomidine administered high dose dex Dexmedetomidine 1 mic/kg of dexmedetomidine administered intermediate dose dex Dexmedetomidine 0.75 mic/kg of dexmedetomidine administered
- Primary Outcome Measures
Name Time Method postoperative analgesic duration 24 hours postoperative analgesic duration with each dose
- Secondary Outcome Measures
Name Time Method Pain score 24 hours severity of pain using visual analogue pain score
side effects 24 hours as hemodynamic effect as (hypotension, bradycardia), nausea and vomiting.
dynamic pain score 24 hours Dynamic visual analogue pain score (pain with cough, deep breath, and movement)
Related Research Topics
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Trial Locations
- Locations (1)
Assiut University Hospitals
🇪🇬Assiut, Assiut Governorate, Egypt