Status:
UNKNOWN
Magnesium Sulfate as an Adjuvant to Propofol During Consious Sedation in Colonoscopy
Lead Sponsor:
Assiut University
Conditions:
Magnesium
Intraoperative Analgesia
Eligibility:
All Genders
40-70 years
Phase:
PHASE2
PHASE3
Brief Summary
Colonoscopy is one of the most commonly performed outpatient procedures throughout the world as a screening, diagnostic, and therapeutic tool to evaluate the large intestine from the distal rectum to ...
Detailed Description
Colonoscopy is one of the most commonly performed outpatient procedures throughout the world as a screening, diagnostic, and therapeutic tool to evaluate the large intestine from the distal rectum to ...
Eligibility Criteria
Inclusion
- 1\. The subject is scheduled for elective colonoscopy. 2. The subject is ≥ 40 years and ≤ 70 years. 3. Both sexes. 4.No obvious abnormalities in preoperative ECG, blood routine, electrolytes, and other tests. 5. ASA class 1-3.
Exclusion
- Subject is known or believed to be pregnant or lactating women. 2. Patients are known hypersensitivity to any of the drugs that would be used in the study. 3. Severe cardiac, renal, lung, or liver diseases. 4. Hypotension (systolic blood pressure\< 90 mm Hg), uncontrolled hypertension (systolic blood pressure\> 170 mmHg, diastolic blood pressure\> 100mmHg). 5. Chronic Opioid Use (daily or almost daily use of opioids for\> 3 months). 6. Patients that are immunologically compromised. 7. Sleep apnea syndrome or difficult airway. 8. preexisting hypoxemia (Spo2\< 90 %). 9. History of adverse events with prior sedation. Additionally, patients who had taken any sedative drugs within the previous 24h
Key Trial Info
Start Date :
January 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2025
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT06131905
Start Date
January 1 2024
End Date
December 1 2025
Last Update
December 18 2023
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