Actively Recruiting
Registry for Patients Receiving Intravenous Nutrition at Home
Led by University Health Network, Toronto · Updated on 2022-11-04
1000
Participants Needed
10
Research Sites
1252 weeks
Total Duration
On this page
Sponsors
U
University Health Network, Toronto
Lead Sponsor
C
Canadian Nutrition Society
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of study is to build a Canadian HTPN Registry to collect pertinent demographic and clinical data on the HTPN population in Canada and to determine the factors affecting survival, complications and TPN-dependency. These results will help establish standards of practice and develop future multi-center studies. This will greatly benefit the HTPN patient population.
CONDITIONS
Official Title
Registry for Patients Receiving Intravenous Nutrition at Home
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with long-term administration of home total parenteral nutrition
- Age greater than 18 years
You will not qualify if you...
- None
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 10 locations
1
Foothills Medical Centre
Calgary, Alberta, Canada
Actively Recruiting
2
Captial Health/University Of Alberta
Edmonton, Alberta, Canada
Actively Recruiting
3
BC Home Parenteral Nutrition Program
Vancouver, British Columbia, Canada
Actively Recruiting
4
St. Boniface General Hospital
Winnipeg, Manitoba, Canada, R2H 2A6
Actively Recruiting
5
Hamilton Health Sciences
Hamilton, Ontario, Canada
Actively Recruiting
6
St. Michael's Hospital
Toronto, Ontario, Canada
Actively Recruiting
7
Hopital St-Luc
Montreal, Quebec, Canada, H2X 0C1
Actively Recruiting
8
McGill University
Montreal, Quebec, Canada, H3G 1A4
Actively Recruiting
9
Hotel-Dieu de Quebec
Québec, Quebec, Canada
Actively Recruiting
10
Saskatchewan Adult HTPN Program
Regina, Saskatchewan, Canada, S4T 1A5
Actively Recruiting
Research Team
J
Johane Allard, MD,FRCPC
CONTACT
K
Katherine JP Schwenger, BASc, MAN, RD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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