Quality of Life and Symptoms in Patients With Newly Diagnosed Myelodysplastic Syndromes
Status unconfirmed
Conditions studied: Adult, Myelodysplastic Syndromes
In brief
RATIONALE: Gathering information about quality of life, fatigue, and other symptoms from patients with myelodysplastic syndromes may help doctors learn more about the disease and may help plan treatment. PURPOSE: This clinical trial is studying quality of life and symptoms in patients with newly diagnosed myelodysplastic syndromes.
Key facts
- Study ID
- NCT00809575
- Run by
- Gruppo Italiano Malattie EMatologiche dell'Adulto
- People needed
- 927
- Starts
- 2008-10-02
- Expected to finish
- 2021-02-01
- Last updated by the study team
- 2020-12-22
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with newly diagnosed myelodysplastic syndrome (MDS) according to WHO classification with any known IPSS risk score category. The initial diagnosis of MDS is acceptable within 3 months before date of registration.
- Having a full baseline QoL Evaluation completed (i.e. EORTC QLQ-C30; EQ5D; FACIT-Fatigue and Control Preference Scale).
- Adult patients (≥ 18 years old).
- Written informed consent provided.
You may not qualify if…
- Patients who have received prior treatment other than platelets or RBC transfusions, iron chelation, antibiotic/virostatic drugs, vitamins;
- Patients with therapy related MDS.
- Having any kind of psychiatric disorder or major cognitive dysfunction.
- Not able to read and understand local language.
Where it is running
- The University of Texas, MD Anderson Cancer Center — Houston, Texas, United States
- Innsbruck University Hospital — Innsbruck, Austria
- ZNA Middelheim — Antwerp, Belgium
- AZ Sint-Jan AV, Department of Hematology — Bruges, Belgium
- CH Jolimont — Brussels, Belgium
- CHC - Centre Hospitalier Chrétien — Liège, Belgium
- Curitiba Unidade de Hematologia - Hemoterapia e Oncologia. Setor de Transplante de Medula Ossea. Complexo Hospital de Clinicas da Universidade Federal do Parana (CHC-UFPR) — Curitiba, Brazil
- Affiliated Hospital of Liaoning University of Traditional Chinese Medicine — China, China
- Kunming Medical University — Kunming, China
- Hematology - Clinical Hospital Centre Rijeka - Faculty of Medicine - University of Rijeka — Rijeka, Croatia
- General Teaching Hospital — Prague, Czechia
- Saint - Cloud Medecin des CLCC Hematologie Service E Hopital ReneHuguenin - Institut Curie — Saint-Cloud, France
- Purpan Hospital - Internal Medicine Department — Toulouse, France
- Department of Hematology - Universitatsklinikum Carl Gustav Carus — Dresden, Germany
- University of Freiburg Medical Center — Freiburg im Breisgau, Germany
- Istituto di Ematologia - IRCCS Ospedale Casa Sollievo della Sofferenza — San Giovanni Rotondo, Foggia, Italy
- U.O.A. di Medicina Trasfusionale e DH di Ematologia - ASL TO 4 Ospedale di Ivrea — Ivrea, Torino, Italy
- Asl Di Asti - Ospedali Riuniti - Presidio Ospedaliero Cardinal G. Massaia - Sc Oncologia — Asti, Italy
- Unità Operativa Ematologia 1 - Università degli Studi di Bari — Bari, Italy
- ASL N.8 - Ospedale "A. Businco" - Unità Operativa di Ematologia e Trapianto di Midollo — Cagliari, Italy
- CTMO - Ematologia - Ospedale "Binaghi" — Cagliari, Italy
- Ospedale "Ferrarotto" — Catania, Italy
- A.O. Pugliese Ciaccio — Catanzaro, Italy
- Aou Arcispedale Sant'Anna - Uoc Ematologia E Fisiopatologia Della Coagulazione — Cona, Italy
- Memorial Sloan-Kettering Cancer Center (MSKCC) — New York, New York, United States
Full record on ClinicalTrials.gov
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