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  1. 1. Test clinico
  2. 2. Documentazione di routine
  3. 3. Registro / studio di coorte
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Eligibility NCT00528567 Breast Cancer - Eligibility

- 10/12/13 - 1 modulo, 2 itemgroups, 8 elementi, 2 lingue
Itemgroups: Inclusion Criteria, Exclusion Criteria
ODM derived from http://clinicaltrials.gov/show/NCT00528567

Eligibility NCT00130858 # Soft Tissue Sarcoma - Eligibility

- 09/12/13 - 1 modulo, 3 itemgroups, 17 elementi, 2 lingue
Itemgroups: Inclusion criteria, Exclusion criteria, Medical Concepts
Phase II Study to evaluate the response on two blocks of topotecan and carboplatin

Eligibility NCT00642941 Sarcoma - Eligibility

- 09/12/13 - 1 modulo, 2 itemgroups, 8 elementi, 2 lingue
Itemgroups: Inclusion Criteria, Exclusion Criteria
ODM derived from http://clinicaltrials.gov/show/NCT00642941

Eligibility NCT00655252 Metastatic Renal Cell Cancer - Eligibility

- 09/12/13 - 1 modulo, 2 itemgroups, 10 elementi, 2 lingue
Itemgroups: Inclusion Criteria, Exclusion Criteria
ODM derived from http://clinicaltrials.gov/show/NCT00655252

Eligibility DRKS00009647 NCT00036543 Prostate Cancer - Eligibility

- 09/12/13 - 1 modulo, 3 itemgroups, 11 elementi, 2 lingue
Itemgroups: Inclusion criteria, Exclusion criteria, Medical Concepts
A Study of Atrasentan in Men With Metastatic, Hormone-Refractory Prostate Cancer Inclusion Criteria: - Diagnosis of prostate cancer. - Rising PSA while on hormonal therapy or following surgical castration. - Documented evidence of metastatic disease. Exclusion Criteria: - Have received cytotoxic chemotherapy. - Have received opioid or narcotic medications (such as codeine or morphine) or radiation for pain caused by your prostate cancer in the last 6 months

Eligibility NCT00684619 T-ALL, T-NHL (Lymphoblastic) - Eligibility

- 09/12/13 - 1 modulo, 2 itemgroups, 15 elementi, 2 lingue
Itemgroups: Inclusion Criteria, Exclusion Criteria
ODM derived from http://clinicaltrials.gov/show/NCT00684619

Eligibility NCT00785330 Non-Hodgkin's Lymphoma - Eligibility

- 09/12/13 - 1 modulo, 2 itemgroups, 11 elementi, 2 lingue
Itemgroups: Inclusion Criteria, Exclusion Criteria
ODM derived from http://clinicaltrials.gov/show/NCT00785330

Eligibility NCT00796757 Renal Cell Cancer - Eligibility

- 09/12/13 - 1 modulo, 2 itemgroups, 10 elementi, 2 lingue
Itemgroups: Inclusion Criteria, Exclusion Criteria
ODM derived from http://clinicaltrials.gov/show/NCT00796757

HIS pathology documtation cancer conference breast cancer - HIS

- 07/08/13 - 1 modulo, 3 itemgroups, 35 elementi, 2 lingue
Itemgroups: Admininstrative Daten, Pathologie-Dokumentation für FK Tumorboard, Pathologische TNM-Stadium
HIS form from Soarian. "Frauenklinik Erlangen" with friendly permission of the gynecology Erlangen (Prof. Beckmann) and the medical informatics department Erlangen (PD Dr. Bürkle)

HIS documentation cancer conference - gynecology breast cancer - HIS

- 07/08/13 - 1 modulo, 8 itemgroups, 86 elementi, 2 lingue
Itemgroups: Admininstrative Daten, Dokumentation TB Mamma, klin. TNM-Stadium, vorh. path.TNM-Stadium, TNM-Stadium der Patho, endgültiges TNM-Stadium, Geplante Therapie, Weiteres
HIS form from Soarian. "Frauenklinik Erlangen" with friendly permission of the gynecology Erlangen (Prof. Beckmann) and the medical informatics department Erlangen (PD Dr. Bürkle)

dataset minimal dataset DPKK prostate cancer - dataset

- 07/08/13 - 1 modulo, 9 itemgroups, 49 elementi, 2 lingue
Itemgroups: Datenelemente I, Topographie, Datenelemente II, PSA, Datenelemente III, Art der durchgeführten Operation, Datenelemente IV, Histomorphologie des Prostatektomiepräparates, Datenelemente V
with friendly permission, http://www.dpkk.de, Minimaldatensatz des DPKK

Pre-Study - NCI Standard Registration Template - 2745056v1.0 - NCI Standard Registration Template

- 20/09/12 - 1 modulo, 3 itemgroups, 18 elementi, 1 linguaggio
Itemgroups: Mandatory Registration Questions, Conditional Registration Questions, Optional Registration Questions
The collection of CDEs used in the registration module. Registration consists of the registering institution applying for entry of a consented participant into a specific research study by conveying designated registration information to a central facility that is in charge of accepting participants into the study. Source Form: NCI FormBuilder: https://formbuilder.nci.nih.gov/FormBuilder/formDetailsAction.do?method=getFormDetails&formIdSeq=4C056DEC-99CB-35E0-E044-0003BA3F9857

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