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Symptom Experience of Multiple Myeloma Patients Treated with Autologous Stem Cell Transplantation Following High Dose Chemotherapy

Symptom Experience of Multiple Myeloma Patients Treated with Autologous Stem Cell Transplantation Following High Dose Chemotherapy - syMMex

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00004345
Enrollment
40
Registered
2013-01-30
Start date
2012-12-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

C90

Interventions

Group 1: All Patients with multiple myeloma, 18 years of age and older admitted to one of the three transplant wards of the Department of Hematology/Oncology, University Medical Center, Freiburg, Germ

Sponsors

Universitätsklinikum Freiburg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: All Patients with MM, and 18 years of age and older admitted to one of the three transplant wards of the Department of Hematology/Oncology, University Medical Center, Freiburg, Germany, for HD and ASCT will be screened for inclusion criteria and consecutively included in the study. The criteria for inclusion are that the patients are able to read, understand, and answer the PROVIVO questionnaire and that HD and ASCT is part of the first treatment regimen after diagnosis.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Symptom experience of patients will be measured with the PROVIVO questionnaire at four timepoints: admission (day -4, calculated from day of ASCT), nadir (moment of lowest count of white blood cells, about day +7 to +10), discharge (about day +15) and one month after discharge of HD and ASCT (30 days after discharge).

Secondary

MeasureTime frame
Evaluation of the PROVIVO questionnaire for the use with patients with multiple myeloma and HD and ASCT

Countries

Germany

Contacts

Public ContactMatthias Naegele

Universitätsklinikum Freiburg

matthias.naegele@uniklinik-freiburg.de076127034190

Outcome results

None listed

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