search  
 


Home

Who are we?

Why
register?


Signup for
registration


Online registration

Log in to register
your trial


Search a trial

NRT en CCMO

Contact

NEDERLANDS





MetaRegister
van CCT (UK)


ISRCTN-Register
van CCT (UK)


Home treatment for haemophilia patients.


- candidate number8919
- NTR NumberNTR2686
- ISRCTNISRCTN wordt niet meer aangevraagd.
- Date ISRCTN created
- date ISRCTN requested
- Date Registered NTR10-jan-2011
- Secondary IDs10-269/ C METC UMCU
- Public TitleHome treatment for haemophilia patients.
- Scientific TitleHome treatment in prophylaxis for haemophilia: A quantitative assessment.
- ACRONYMQAHT-study
- hypothesisThe primary objective is to quantify the learning process of self infusion and the self infusion procedure.
- Healt Condition(s) or Problem(s) studiedHome treatment, Haemophilia, Prophylaxis, Intravenous infusion, Learningprocess
- Inclusion criteria1. All haemophilia or Von Willebrand type III patients or caretakers of children (with or without CVAD) treated with prophylaxis (possible learning for self infusion);
2. Patients who are treated at the van Creveldkliniek Utrecht, Haemophilia Treatment Centre Amsterdam, or Erasmus Medical Centre Rotterdam, in the estimated period from of 3 years.
- Exclusion criteriaPatients who are treated on demand.
- mec approval receivedyes
- multicenter trialyes
- randomisedno
- groupParallel
- TypeSingle arm
- Studytypeobservational
- planned startdate 1-sep-2010
- planned closingdate1-sep-2013
- Target number of participants175
- InterventionsThis study comprises a retro- and prospective observational study which is combined with a nursing consultation. The present project will expand the regular nursing consultation with a history, timing of infusion and an introduction of home-visits to patients who are using home-treatment since more than 1 year.
- Primary outcomeQuantification of the learning process of self infusion and the self infusion procedure, that will serve as a base-line for futher research to improve adherence.
- Secondary outcome1. Time needed to learn to administer prophylaxis;
2. Timing of self infusion;
3. Proportion of infusions taken in the mornings in comparison with the bleeding frequency;
4. Age at which transition takes place.
- TimepointsData collection:
1. For research on self infusion: 3 years;
2. Retrospective data: 0.3 years.

Data Analysis: 0.5 years;
Report: 0.5 years.
- Trial web sitehttp://www.umcutrecht.nl/subsite/vancreveldkliniek/Onderzoek/
- statusopen: patient inclusion
- CONTACT FOR PUBLIC QUERIES L.H. Schrijvers
- CONTACT for SCIENTIFIC QUERIES L.H. Schrijvers
- Sponsor/Initiator University Medical Center Utrecht (UMCU)
- Funding
(Source(s) of Monetary or Material Support)
Baxter Healthcare Corporation
- PublicationsN/A
- Brief summaryThe primary objective of this retro/prospective observational study, is to quantify the process of Home treatment for haemophilia patients. The datacollection is combined with the regular nursing consultation.
- Main changes (audit trail)
- RECORD10-jan-2011 - 21-jan-2011


  • Indien u gegevens wilt toevoegen of veranderen, kunt u een mail sturen naar nederlands@trialregister.nl