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Clinical Trials in Egypt / NCT06808295
Recruiting Phase 1

Dexmedetomidine an Effective Drug in Reducing Anesthetic Requirements in External Dacrocystorhinostomy (DCR) Patients

NCT06808295 · tracked via the Priya Life Science Egypt tracker
Sponsor
Research Institute of Ophthalmology, Egypt
Phase
Phase 1
Started
2024-04-16
Last updated
2025-02-05

Condition(s) studied

Patients Undergoing External Dacrocystorhinostomy OperationsAssess Decreased Anesthetic Requirements Intraoperative

Investigational drug(s) / intervention(s)

Dexmedetomidine Hydrochloride →

Dexmedetomidine Hydrochloride: drug will be given before induction and anesthetic doses and hemodynamics will be assessed pre- intra and postoperative

Study summary

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

Eligibility

Sex
ALL
Min age
16 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: patients of both sexes 16 years to 75 years of age ASA (American society of Anesthesiologists) I-III Exclusion Criteria: * Pediatric age group * ASA more than III

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Research Institute of Ophthalmolgy Giza Egypt Recruiting

More Research Institute of Ophthalmology, Egypt trials in Egypt

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06808295 on ClinicalTrials.gov ↗ ← All trials in Egypt