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CAre of Patients With PArenteral Nutrition At Home (CAPANAH)

This study has been completed.
Sponsor:
Collaborators:
Ziekenhuis Netwerk Antwerpen (ZNA)
AZ Sint-Lucas
Universiteit Antwerpen
AZ Sint-Blasius Dendermonde
Imelda Hospital, Bonheiden
Ziekenhuis Oost-Limburg
AZ Damiaan, Oostende
H.-Hartziekenhuis Roeselare-Menen vzw
Universitair Ziekenhuis Brussel
University Hospital, Ghent
Jessa Hospital
Information provided by (Responsible Party):
Mira Dreesen, PhD student, Katholieke Universiteit Leuven
ClinicalTrials.gov Identifier:
NCT01545063
First received: March 1, 2012
Last updated: July 18, 2017
Last verified: July 2017
March 1, 2012
July 18, 2017
May 2012
April 2013   (Final data collection date for primary outcome measure)
  • Quality of life [ Time Frame: 2 years ]
    Quality of life will be investigated with the HPN-QoL(r) or FACIT-G (r).
  • Number of catheter related infections [ Time Frame: 2 years ]
Same as current
Complete list of historical versions of study NCT01545063 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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Not Provided
 
CAre of Patients With PArenteral Nutrition At Home
Prospective Non-interventional Non-controlled Multicenter Observational Study to Evaluate the Quality of Care for Adult Patients on Home Parenteral Nutrition (HPN)

This research aims to give an overview of a number of aspects related to the quality of care for adult patients on home parenteral nutrition.

Concretely this study follows up different aspects on different moments in the care of the patient pathways:

  • process indicators concerning indication, parenteral nutrition, training, team access roads and the succession of complications
  • Outcome indicators
  • the health-related quality of life
  • discrepancies in medication use
  • the role of the different health care providers

Adult patients on HPN will be contacted by phone at three different time moments after their discharge to ask them about indicators, quality of life and discrepancies in medication use. After the follow-up, medical dossiers will be consulted to know which indicators are followed in practice.

The role of the different health care providers will be investigated by face-to-face interviews with different healthcare professionals.

Observational
Observational Model: Other
Time Perspective: Prospective
Not Provided
Not Provided
Probability Sample
Adult HPN patients with peritoneal carcinomatosis with intestinal occlusion or with crohn's disease, radiation enteritis, chronic diarrhea, intestinal lymphomas.
  • Crohn's Disease
  • Peritoneal Carcinomatosis With Intestinal Occlusion
  • Radiation Enteritis
  • Chronic Diarrhea
  • Intestinal Lymphomas
Not Provided
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Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
39
April 2013
April 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients in Flanders who speak Dutch, are older then 18 years and are able to give an informed consent.

Exclusion Criteria:

  • Patients who are younger then 18 years.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Belgium
 
 
NCT01545063
S54137
Yes
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Plan to Share IPD: No
Mira Dreesen, PhD student, Katholieke Universiteit Leuven
Katholieke Universiteit Leuven
  • Ziekenhuis Netwerk Antwerpen (ZNA)
  • AZ Sint-Lucas
  • Universiteit Antwerpen
  • AZ Sint-Blasius Dendermonde
  • Imelda Hospital, Bonheiden
  • Ziekenhuis Oost-Limburg
  • AZ Damiaan, Oostende
  • H.-Hartziekenhuis Roeselare-Menen vzw
  • Universitair Ziekenhuis Brussel
  • University Hospital, Ghent
  • Jessa Hospital
Not Provided
Katholieke Universiteit Leuven
July 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP