Research Institute of Ophthalmolgy
Giza, Egypt
Location status: Recruiting
NCT Number: NCT06808295
Assessing the intra and postoperative hemodynamic stability in patients undergoing external dacrocystorhinostomy under general anesthesia using Dexmedetomidine as a preoperative sedation compared to traditional technique with intraoperative analgesia and assessing decreased anesthetic requirements intra and postoperative
Interested in participating?
Request Info16 year–75 year
All sexes
Interventional
Phase 1
Giza, Egypt
Location status: Recruiting
Dexmedetomidine is a highly selective alpha 2 adrenoceptor agonist, having characteristics of natural sleep like sedation, can reduce pain intensity and opioid consumption without influencing the time of recovery from general anesthesia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
patients of both sexes 16 years to 75 years of age ASA (American society of Anesthesiologists) I-III
Exclusion criteria
drug will be given before induction and anesthetic doses and hemodynamics will be assessed pre- intra and postoperative
Time frame: from 20 minutes after administering the drug till 2 hours after full recovery
Measuring the heart rate and the blod pressure every 5 minutes intraoperative and for half an hour postoperative to assess hemodynamic stability
Time frame: from 20 minutes after administering the drug till 2 hours after full recovery
Reducing postoperative delirium in elderly patients
Contact information is provided by the study sponsor or research team.
Research Institute of Ophthalmology, Egypt
Other
Dexmedetomidine As an Effective Drug in Reducing Anesthetic Requirements in Patients Undergoing External Dacrocystorhinostomy, a Randomized Controlled Study
Acronym: DCR
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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.