Dexmedetomidine in Sonographic Guided Erector Spinae Plane Block
NCT ID: NCT06899841
Last Updated: 2025-03-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE2/PHASE3
90 participants
INTERVENTIONAL
2024-10-01
2026-04-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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low dose dex
0.5 mic/kg of dexmedetomidine administered
Dexmedetomidine
different doses of dexmedetomidine added to bupivacaine in erector spinae plane block
intermediate dose dex
0.75 mic/kg of dexmedetomidine administered
Dexmedetomidine
different doses of dexmedetomidine added to bupivacaine in erector spinae plane block
high dose dex
1 mic/kg of dexmedetomidine administered
Dexmedetomidine
different doses of dexmedetomidine added to bupivacaine in erector spinae plane block
Interventions
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Dexmedetomidine
different doses of dexmedetomidine added to bupivacaine in erector spinae plane block
Eligibility Criteria
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Inclusion Criteria
* 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.
Exclusion Criteria
* 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.
18 Years
70 Years
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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Mahmoud Faisal
dr
Locations
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Assiut University Hospitals
Asyut, Assiut Governorate, Egypt
Countries
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Facility Contacts
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Other Identifiers
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04-2024-200943
Identifier Type: -
Identifier Source: org_study_id
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