CAre of Patients With PArenteral Nutrition At Home (CAPANAH)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified May 2012 by Katholieke Universiteit Leuven.
Recruitment status was  Recruiting
Sponsor:
Collaborators:
Ziekenhuis Netwerk Antwerpen (ZNA)
AZ Sint-Lucas Brugge
Universiteit Antwerpen
AZ Sint-Blasius Dendermonde
Imelda Hospital, Bonheiden
Ziekenhuis Oost-Limburg
AZ Sint-Lucas & Volkskliniek, Gent
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: May 25, 2012
Last verified: May 2012

March 1, 2012
May 25, 2012
May 2012
May 2013   (final data collection date for primary outcome measure)
  • Quality of life [ Time Frame: 2 years ] [ Designated as safety issue: No ]
    Quality of life will be investigated with the HPN-QoL(r) or FACIT-G (r).
  • Number of catheter related infections [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01545063 on ClinicalTrials.gov Archive Site
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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
Time Perspective: Prospective
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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
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
120
December 2013
May 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.
Both
18 Years and older
No
Belgium
 
NCT01545063
S54137
Yes
Mira Dreesen, PhD student, Katholieke Universiteit Leuven
Katholieke Universiteit Leuven
  • Ziekenhuis Netwerk Antwerpen (ZNA)
  • AZ Sint-Lucas Brugge
  • Universiteit Antwerpen
  • AZ Sint-Blasius Dendermonde
  • Imelda Hospital, Bonheiden
  • Ziekenhuis Oost-Limburg
  • AZ Sint-Lucas & Volkskliniek, Gent
  • AZ Damiaan, Oostende
  • H.-Hartziekenhuis Roeselare-Menen vzw
  • Universitair Ziekenhuis Brussel
  • University Hospital, Ghent
  • Jessa Hospital
Not Provided
Katholieke Universiteit Leuven
May 2012

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