Informations:
Erreur:
ID
13676
Description
A 48-Week (24-Week Baseline Followed by a 24-Week Treatment) Phase II Pilot Study of the Tolerability and Effect/Efficacy of Subcutaneously Administered Insulin-Like Growth Factor-1 (rhIGF) (CEP-151) in Multiple Sclerosis (MS) Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00001669
Lien
https://clinicaltrials.gov/show/NCT00001669
Mots-clés
Versions (1)
- 27/02/2016 27/02/2016 -
Téléchargé le
27 février 2016
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT00001669
Eligibility Multiple Sclerosis NCT00001669
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Sclerosis NCT00001669
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Multiple sclerosis, disease stage, frequency
Item
stage i - known by history to have a mean enhancing lesion frequency of 0.3 per month or greater;
boolean
C0026769 (UMLS CUI [1])
C0699749 (UMLS CUI [2])
C0699749 (UMLS CUI [2])
Multiple sclerosis, disease stage, frequency
Item
stage ii - known by history to have a mean enhancing lesion frequency of 0.5 per month or greater;
boolean
C0026769 (UMLS CUI [1])
C0699749 (UMLS CUI [2])
C0699749 (UMLS CUI [2])
comply with protocol
Item
ability to comply with protocol requirements;
boolean
C1321605 (UMLS CUI [1])
written informed consent
Item
provide written informed consent;
boolean
C0021430 (UMLS CUI [1])
Gender, childbearing potential, pregnancy, breast feeding, contraception
Item
if a female patient, not of child bearing potential (surgically sterilized or post-menopausal) or if of child bearing potential, documented to be nonpregnant by urine pregnancy test and not lactating with adequate contraception and counseling.
boolean
C0079399 (UMLS CUI [1])
C3831118 (UMLS CUI [2])
C0032961 (UMLS CUI [3])
C0006147 (UMLS CUI [4])
C0700589 (UMLS CUI [5])
C3831118 (UMLS CUI [2])
C0032961 (UMLS CUI [3])
C0006147 (UMLS CUI [4])
C0700589 (UMLS CUI [5])
Gender, contraception
Item
male patients should also receive adequate counseling and exercise adequate contraception.
boolean
C0079399 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0700589 (UMLS CUI [2])
prestudy assessment
Item
no clinically significant abnormalities on the prestudy laboratory evaluations, physical examination, electrocardiogram (ecg), chest x-ray, mammogram or ophthalmologic exam.
boolean
C3899485 (UMLS CUI [1])
connective tissue or rheumatic disorder
Item
no connective tissue or rheumatic disorder (systemic lupus erythematosus [sle] ; rheumatoid arthritis [ra]; progressive systemic sclerosis [pss]; sjogren's syndrome [ss]).
boolean
C0009782 (UMLS CUI [1])
C3495832 (UMLS CUI [2])
C3495832 (UMLS CUI [2])
hiv, htlv-1, hep b or c
Item
patient may not be hiv (human immunodeficiency virus), htlv-1 (human t cell leukemia virus), or hb/c ag (hepatitis b or c surface antigen) positive.
boolean
C0019682 (UMLS CUI [1])
C0020094 (UMLS CUI [2,1])
C0019163 (UMLS CUI [2,2])
C0019196 (UMLS CUI [3])
C0020094 (UMLS CUI [2,1])
C0019163 (UMLS CUI [2,2])
C0019196 (UMLS CUI [3])
history of insulin-producing tumors or reactive hypoglycemia
Item
no history of insulin-producing tumors or reactive hypoglycemia.
boolean
C0021670 (UMLS CUI [1])
C0271710 (UMLS CUI [2])
C0271710 (UMLS CUI [2])
clinically significant medical condition
Item
no clinically significant medical condition (e.g., within 6 months of screen had myocardial infarction, angina pectoris, untreated hypertension, and/or congestive heart failure [chf] that, in the opinion of the investigator would compromise the safety of the patient.
boolean
C0009488 (UMLS CUI [1])
MRI complications
Item
ability to tolerate mri examinations due to claustrophobia, or have contraindications to mri scanning, such as pacemakers, aneurysm clips, or shrapnel fragments. welders and metal workers must have radiographic evidence to document lack of foreign bodies in the eyes or they will be excluded, due to the risk of eye injury while in the mri machine.
boolean
C1321605 (UMLS CUI [1])
C0024485 (UMLS CUI [2])
C0024485 (UMLS CUI [2])
substance use disorder
Item
no history of substance use disorder (dsm-iv criteria) within the past two years.
boolean
C0038586 (UMLS CUI [1])
type i or type ii diabetes treated with hypoglycemic agents
Item
no type i or type ii diabetes treated with hypoglycemic agents (diet-controlled type ii diabetes may be included.)
boolean
C0011849 (UMLS CUI [1])
C0020616 (UMLS CUI [2])
C0020616 (UMLS CUI [2])
malignancies
Item
no history of cancer (with the exception of localized skin cancers with no evidence of metastasis, significant invasion, or recurrence) within three years of screening.
boolean
C0006826 (UMLS CUI [1])
relatives with breast cancer
Item
no first or second degree relatives with breast cancer.
boolean
C0559119 (UMLS CUI [1])
investigational drug use
Item
have not used an investigational drug within 30 days of the screen visit.
boolean
C0013230 (UMLS CUI [1])
Immunosuppressive agents
Item
have previously received interferon-alpha, interferon-beta, copolymer 1, cyclophosphamide, intravenous immunoglobulin, oral myelin, or other immunosuppressive drugs within 6 months of screen.
boolean
C0021081 (UMLS CUI [1])