Assiut University Hospitals
Asyut, Assiut Governorate, 71111, Egypt
Location status: Recruiting
NCT Number: NCT06899841
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.
Interested in participating?
Request Info18 year–70 year
All sexes
Interventional
Phase 2 / Phase 3
Asyut, Assiut Governorate, 71111, Egypt
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
different doses of dexmedetomidine added to bupivacaine in erector spinae plane block
Time frame: 24 hours
postoperative analgesic duration with each dose
Time frame: 24 hours
severity of pain using visual analogue pain score
Time frame: 24 hours
as hemodynamic effect as (hypotension, bradycardia), nausea and vomiting.
Time frame: 24 hours
Dynamic visual analogue pain score (pain with cough, deep breath, and movement)
Assiut University
Other
Effect of Different Doses of Dexmedetomidine Added to Local Anesthetic in Sonographic Guided Erector Spinae Plane Block for Pain Management After Renal Surgeries : Randomized Clinical Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07695987
Agnosia, Nervous System Diseases
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT07716540
Agnosia, Nervous System Diseases
Istanbul, Turkey (Türkiye)
View Trial DetailsNCT07226700
Agnosia, JOURNAVX
New York, United States
View Trial DetailsNCT07707609
Agnosia, Chronic Disease
Hyderabad, Telangana, India
View Trial Details