Trials / Recruiting
RecruitingNCT07066605
The Effect of Dexmedetomidine on Agitation During Weaning From Mechanical Ventilation
The Effect of Dexmedetomidine on Agitation During Weaning From Mechanical Ventilation in Critically Ill Patients"
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 62 (estimated)
- Sponsor
- Sohag University · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to evaluate the effect of dexmedetomidine on the level of agitation during the weaning process from mechanical ventilation in critically ill patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Group A (Dexmedetomidine Group) | patients will receive dexmedetomidine infusion starting at 0.2 mcg/kg/hr. |
| DRUG | Group B (Control Group) | patients will receive standard ICU sedation protocol without dexmedetomidine (e.g., fentanyl) |
Timeline
- Start date
- 2025-06-13
- Primary completion
- 2025-12-30
- Completion
- 2025-12-30
- First posted
- 2025-07-15
- Last updated
- 2025-07-15
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT07066605. Inclusion in this directory is not an endorsement.