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  1. 1. Klinische Studie
  2. 2. Routinedokumentation
  3. 3. Register-/Kohortenstudien
  4. 4. Qualitätssicherung
  5. 5. Datenstandard
  6. 6. Patientenfragebogen
  7. 7. Medizinische Fachrichtung
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WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 2 Week 8 (V9) 2009-011417-24 DRKS00000657 - WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 2 Week 8 (V9) 2009-011417-24

- 23.11.16 - 1 Formular, 1 Itemgruppe, 15 Datenelemente, 1 Sprache
Itemgruppe: Vital signs
Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 2 Week 7 (V8) 2009-011417-24 DRKS00000657 - WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 2 Week 7 (V8) 2009-011417-24

- 23.11.16 - 1 Formular, 1 Itemgruppe, 15 Datenelemente, 1 Sprache
Itemgruppe: Vital signs
Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 2 Week 6 (V7) 2009-011417-24 DRKS00000657 - WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 2 Week 6 (V7) 2009-011417-24

- 23.11.16 - 1 Formular, 1 Itemgruppe, 16 Datenelemente, 1 Sprache
Itemgruppe: Vital signs
Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 5 (V6) 2009-011417-24 DRKS00000657 - WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 5 (V6) 2009-011417-24

- 23.11.16 - 1 Formular, 1 Itemgruppe, 16 Datenelemente, 1 Sprache
Itemgruppe: Vital signs
Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 4 (V5) 2009-011417-24 DRKS00000657 - WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 4 (V5) 2009-011417-24

- 23.11.16 - 1 Formular, 1 Itemgruppe, 15 Datenelemente, 1 Sprache
Itemgruppe: Vital signs
Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 2 (V3) 2009-011417-24 DRKS00000657 - WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 2 (V3) 2009-011417-24

- 23.11.16 - 1 Formular, 1 Itemgruppe, 17 Datenelemente, 1 Sprache
Itemgruppe: Vital signs
Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 3 (V4) 2009-011417-24 DRKS00000657 - WTZ-GIST-09-01 (Imatinib + LBH589) Cycle 1 Week 3 (V4) 2009-011417-24

- 23.11.16 - 1 Formular, 1 Itemgruppe, 15 Datenelemente, 1 Sprache
Itemgruppe: Vital signs
Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

DE MS Sub Lok TSP University Hospital Muenster (UKM) Subform

- 23.11.16 - 1 Formular, 4 Itemgruppen, 28 Datenelemente, 1 Sprache
Itemgruppen: Localisation and measures of wound 1, Localisation and measures of wound 2, Localisation and measures of wound 3, Multiple wounds
Hospital Routine Documentation Subform at the University Hospital Muenster. Original Form name: DE MS Sub Lok TSP.

Menstruation Sub University Hospital Muenster (UKM) Subform

- 23.11.16 - 1 Formular, 1 Itemgruppe, 8 Datenelemente, 1 Sprache
Itemgruppe: Gynecological observation
Hospital Routine Documentation Subform at the University Hospital Muenster. Original Form name: Menstruation Sub.

Physical Examination: CRF Wisconsin Madison

- 17.11.16 - 1 Formular, 4 Itemgruppen, 21 Datenelemente, 1 Sprache
Itemgruppen: Header, Physical Examination, Body System, Other
ODM Form derived from: https://ictr.wisc.edu/CaseReptTempt. Template Name: Physical Examination. Case Report Form (CRF)/Source Document templates were created for University of Wisconsin-Madison researchers. These templates are consistent with the FDA's CDASH (Clinical Data Acquisition Standards Harmonization) standards. The CDASH standards identify those elements that should be captured on a Case Report Form (CRF). The forms serve only as templates, and must be edited to meet the study data collection needs as described in the protocol.

Wunddokumentation Sub University Hospital Muenster (UKM) Subform

- 17.11.16 - 1 Formular, 4 Itemgruppen, 51 Datenelemente, 1 Sprache
Itemgruppen: Wound description, Wound healing phase, Exudation, Further factors
Hospital Routine Documentation Subform at the University Hospital Muenster. Original Form name: Wunddokumentation Sub.

AN MS MEDD Anamnese KU University Hospital Muenster (UKM) Subform

- 13.11.16 - 1 Formular, 5 Itemgruppen, 123 Datenelemente, 1 Sprache
Itemgruppen: Allgemeine Angaben, Allgemeine Anamnese, Soziale Anamnese, Vegetative Anamnese, Klinische Untersuchung
Hospital Routine Documentation Form at the University Hospital Muenster. Original Form name: AN MS MEDD Anamnese KU

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