Pico-Salax Colonic Preparation Study: Quantifying Electrolyte and Volume Status Changes
- Registration Number
- NCT00885430
- Lead Sponsor
- Queen's University
- Brief Summary
Twenty adult volunteers will be administered Pico-Salax in the usual fashion for colonoscopy with intense monitoring of serum and urine chemistry and hemodynamics.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- healthy volunteers older than 45
Exclusion Criteria
- impaired renal function
- congestive heart failure ascites known electrolyte abnormalities
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Pico-Salax Pico-Salax -
- Primary Outcome Measures
Name Time Method serum electrolytes 48 hours patient hemodynamics 48 hours
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hotel Dieu Hospital
🇨🇦Kingston, Ontario, Canada