Satisfaction Clinical Trial
Official title:
Comparison of the Sedative Effects of Dexmedetomidine and Propofol During Peribulbar Anaesthesia in Patients Undergoing Vitrectomy Surgery: A Prospective Randomized Clinical Trial
The aim of the work to compare the Sedative Effects of Dexmedetomidine and Propofol during peribulbar anesthesia in patients undergoing vitrectomy surgery on hemodynamic, respiratory parameters, recovery profile, analgesic effects, post-operative cognitive function, patients satisfaction and adverse events.
Status | Recruiting |
Enrollment | 420 |
Est. completion date | May 1, 2025 |
Est. primary completion date | May 1, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 70 Years |
Eligibility | Inclusion Criteria: - Age between 20-70 years. - Expected time of surgery less than 2 hours Exclusion Criteria: - patients with an initial mini mental state examination (MMSE) score less than 23 - Patients refusing LA - Clotting abnormalities - Impaired mental status - Allergy to any of the study medications - Also, patients were excluded if they had severe cardiac disease, chronic obstructive lung disease, a history of sleep apnea and those who received general anesthesia. |
Country | Name | City | State |
---|---|---|---|
Egypt | Beni Suef University Hospital | Bani Suwayf | Beni Suef |
Lead Sponsor | Collaborator |
---|---|
Beni-Suef University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Patient satisfaction | Patient satisfaction will be also assessed using 7-point Likert-like verbal rating scale. One means extremely dissatisfied and seven means extremely satisfied. | 6 hours after the end of surgery. | |
Secondary | Visual analogue scale | The degree of pain was assessed by using a 10-cm visual analog scale (VAS) for pain where: 0=no pain and 10=intolerable pain | 6 hours after the end of surgery |
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
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