Informations:
Erreur:
ID
31000
Description
A Phase 1 Safety Study of the Intravenous Administration of Thymosin Beta in Healthy Volunteers; ODM derived from: https://clinicaltrials.gov/show/NCT00743769
Lien
https://clinicaltrials.gov/show/NCT00743769
Mots-clés
Versions (1)
- 09/07/2018 09/07/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
9 juillet 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Myocardial Infarction NCT00743769
Eligibility Myocardial Infarction NCT00743769
- StudyEvent: Eligibility
Similar models
Eligibility Myocardial Infarction NCT00743769
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Good health | Absence Other medical condition At risk Patient
Item
in good health with no underlying medical condition that, according to the investigator, would place a subject at risk
boolean
C3813622 (UMLS CUI [1])
C0332197 (UMLS CUI [2,1])
C3843040 (UMLS CUI [2,2])
C1444641 (UMLS CUI [2,3])
C0030705 (UMLS CUI [2,4])
C0332197 (UMLS CUI [2,1])
C3843040 (UMLS CUI [2,2])
C1444641 (UMLS CUI [2,3])
C0030705 (UMLS CUI [2,4])
Informed Consent
Item
having given written informed consent
boolean
C0021430 (UMLS CUI [1])
Malignant Neoplasms
Item
evidence of any malignancy
boolean
C0006826 (UMLS CUI [1])
Tobacco use
Item
use of any tobacco product within 7 years of study entry
boolean
C0543414 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Drug abuse
Item
history of drug abuse
boolean
C0013146 (UMLS CUI [1])
Electrocardiogram abnormal
Item
clinically significant abnormal screening ecg
boolean
C0522055 (UMLS CUI [1])
Abnormal vital signs
Item
abnormal vital signs
boolean
C0277804 (UMLS CUI [1])
Steroid therapy Systemic | Immunotherapy | Cytotoxic therapy | Chemotherapy | Investigational New Drugs | Investigational Medical Device | Topical steroids allowed
Item
use of systemic steroidal therapy), immunotherapy, cytotoxic, chemotherapy or any investigational drug or device within 30 days of study entry. topical steroids are allowed
boolean
C0149783 (UMLS CUI [1,1])
C0205373 (UMLS CUI [1,2])
C0021083 (UMLS CUI [2])
C0677881 (UMLS CUI [3])
C0392920 (UMLS CUI [4])
C0013230 (UMLS CUI [5])
C2346570 (UMLS CUI [6])
C2064827 (UMLS CUI [7,1])
C0683607 (UMLS CUI [7,2])
C0205373 (UMLS CUI [1,2])
C0021083 (UMLS CUI [2])
C0677881 (UMLS CUI [3])
C0392920 (UMLS CUI [4])
C0013230 (UMLS CUI [5])
C2346570 (UMLS CUI [6])
C2064827 (UMLS CUI [7,1])
C0683607 (UMLS CUI [7,2])
Gender | Age | Mammography Absent
Item
women, 40 years of age and above, who have not had a mammography within one year of study entry
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0024671 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0001779 (UMLS CUI [2])
C0024671 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Age | Sigmoidoscopy Absent | Colonoscopy Absent
Item
men and women, 50 years of age and above, who have not had a sigmoidoscopy within 5 years and colonoscopy within 10 years of study entry
boolean
C0001779 (UMLS CUI [1])
C0037075 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0009378 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0037075 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0009378 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])