Comparing the efficacy and safety between Propofol And Dexmedetomidine for sedation in claustrophobic Adults undergoing Magnetic resonance imaging (PADAM)

Not Applicable

Completed

• Conditions: Claustrophobia in adults; Anaesthesiology - Anaesthetics; Mental Health - Anxiety

• Registration Number: ACTRN12616000097448
• Lead Sponsor: Pui-San Loh

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-01-29
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

1.ASA I - II according to American Society of Anaesthesiologist guidelines.
2.Patients age 18 - 70 years old.
3.Known case of claustrophobia or history of anxiety/panic attack during an MRI study
4. Patients who were scheduled to undergo an MRI scan for a medical or surgical problem

Exclusion Criteria

1.Patient related - Patient refusal
BMI >30
Hypotension due to any reasons. (Systolic less than 90 mmHg)
Bradycardia (heart rate less than 50 bpm)
Concurrent medication which increase vagal tone or delay AV conduction (e.g.. digoxin / beta blocker)
Chronic lung disease with saturation on room air <91%
Obstructive sleep apnoea
Requires general anaesthesia
2.Drug related - Allergic history to propofol or dexmedetomidine or related compound
3.MRI related - Any contraindications to MRI
Emergency MRI
Interventional procedures

Study & Design

• Study Type: Interventional
• Study Design: Not specified