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Quality Of Life and compliance after changing immunosuppression regimens

Quality Of Life and compliance after changing immunosuppression regimens: A prospective, single-centre, observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN24752762
Enrollment
100
Registered
2011-04-15
Start date
2011-01-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Immunosuppressive regimens after liver transplantation Surgery Immunosuppressive regimens after liver transplantation

Interventions

In this observational study, compliance and quality of life are monitored in patients whose basic immunosuppressive regimen is changed to a once daily formulation using standardised questionnaires

Sponsors

University Hospital Heidelberg (Germany)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. More than or equal to 12 months after liver transplantation 2. Aged more than or equal to 18 years 3. Change in immunosuppressive regimen to a retard formulation

Exclusion criteria

Exclusion criteria: 1. Intellectual or language barriers in understanding and answering the questionnaires 2. Patients admitted to the hospital

Design outcomes

Primary

MeasureTime frame
Quality of life as measured with the SF-36 health questionnaire

Secondary

MeasureTime frame
Compliance as measured with the BAASIS interview

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026