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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)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01545063
Acronym
CAPANAH
Enrollment
39
Registered
2012-03-06
Start date
2012-05-31
Completion date
2013-04-30
Last updated
2017-07-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Diarrhea, Crohn's Disease, Intestinal Lymphomas, Peritoneal Carcinomatosis With Intestinal Occlusion, Radiation Enteritis

Brief summary

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

Detailed description

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.

Interventions

None listed

Sponsors

Ziekenhuis Netwerk Antwerpen (ZNA)
CollaboratorOTHER
AZ Sint-Lucas Brugge
CollaboratorOTHER
Universiteit Antwerpen
CollaboratorOTHER
AZ Sint-Blasius Dendermonde
CollaboratorUNKNOWN
Imelda Hospital, Bonheiden
CollaboratorOTHER
Ziekenhuis Oost-Limburg
CollaboratorOTHER
AZ Damiaan, Oostende
CollaboratorUNKNOWN
H.-Hartziekenhuis Roeselare-Menen vzw
CollaboratorUNKNOWN
Universitair Ziekenhuis Brussel
CollaboratorOTHER
University Hospital, Ghent
CollaboratorOTHER
Jessa Hospital
CollaboratorOTHER
KU Leuven
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Quality of life2 yearsQuality of life will be investigated with the HPN-QoL(r) or FACIT-G (r).
Number of catheter related infections2 years

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026