ID

31836

Description

A Study Evaluating the Safety and Efficacy of Cura-100 in Subjects With Rheumatoid Arthritis and Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00455208

Lien

https://clinicaltrials.gov/show/NCT00455208

Mots-clés

Versions (1)
  1. 01/10/2018 01/10/2018 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

1 octobre 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Rheumatoid Arthritis NCT00455208

Anglais

Eligibility Rheumatoid Arthritis NCT00455208

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
having a diagnosis of rheumatoid arthritis and osteoarthritis at active stage
Description

Rheumatoid Arthritis | Osteoarthritis

Type de données

boolean

Alias
UMLS CUI [1]
C0003873
UMLS CUI [2]
C0029408
able and willing to comply with study visits and procedures specified in this protocol for at least six months period
Description

Protocol Compliance

Type de données

boolean

Alias
UMLS CUI [1]
C0525058
able to understand and willing to sign and date the written informed consent form prior to admission of the study
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
able and willing to provide adequate information for locator purposes
Description

Consent for release of information

Type de données

boolean

Alias
UMLS CUI [1]
C0511175
able and willing to provide self evaluation information and diagnostic report of arthritis as required for efficacy evaluation
Description

Self-Evaluation Information | Diagnostic report Arthritis | Evaluation

Type de données

boolean

Alias
UMLS CUI [1,1]
C2936633
UMLS CUI [1,2]
C1533716
UMLS CUI [2,1]
C0498033
UMLS CUI [2,2]
C0003864
UMLS CUI [3]
C0220825
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant women
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
over-weighted
Description

Overweight

Type de données

boolean

Alias
UMLS CUI [1]
C0497406
hypertension, or diabetes, or a history of cardiovascular disease or kidney disease, or serious skin allergy or other concurrent clinically significant illness or medical condition (other than arthritis) which, in the viewpoint of the study doctor, may put the subject at a possible risk for participation
Description

Hypertensive disease | Diabetes Mellitus | Cardiovascular Disease | Kidney Disease | Cutaneous hypersensitivity Serious | Comorbidity Study Subject Participation Status At risk | Medical condition Study Subject Participation Status At risk | Exception Arthritis

Type de données

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0011849
UMLS CUI [3]
C0007222
UMLS CUI [4]
C0022658
UMLS CUI [5,1]
C0585186
UMLS CUI [5,2]
C0205404
UMLS CUI [6,1]
C0009488
UMLS CUI [6,2]
C2348568
UMLS CUI [6,3]
C1444641
UMLS CUI [7,1]
C3843040
UMLS CUI [7,2]
C2348568
UMLS CUI [7,3]
C1444641
UMLS CUI [8,1]
C1705847
UMLS CUI [8,2]
C0003864
patients used biologic modifier therapy or currently taking immunosuppressive agents might be excluded
Description

Biological Response Modifiers | Immunosuppressive Agents

Type de données

boolean

Alias
UMLS CUI [1]
C0005525
UMLS CUI [2]
C0021081
unable to spend 3 hours for treatment at the study center
Description

Therapeutic procedure Medical center Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0565990
UMLS CUI [1,3]
C1299582
Retour au début de la page

Similar models

Eligibility Rheumatoid Arthritis NCT00455208

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Rheumatoid Arthritis | Osteoarthritis
Item
having a diagnosis of rheumatoid arthritis and osteoarthritis at active stage
boolean
C0003873 (UMLS CUI [1])
C0029408 (UMLS CUI [2])
Protocol Compliance
Item
able and willing to comply with study visits and procedures specified in this protocol for at least six months period
boolean
C0525058 (UMLS CUI [1])
Informed Consent
Item
able to understand and willing to sign and date the written informed consent form prior to admission of the study
boolean
C0021430 (UMLS CUI [1])
Consent for release of information
Item
able and willing to provide adequate information for locator purposes
boolean
C0511175 (UMLS CUI [1])
Self-Evaluation Information | Diagnostic report Arthritis | Evaluation
Item
able and willing to provide self evaluation information and diagnostic report of arthritis as required for efficacy evaluation
boolean
C2936633 (UMLS CUI [1,1])
C1533716 (UMLS CUI [1,2])
C0498033 (UMLS CUI [2,1])
C0003864 (UMLS CUI [2,2])
C0220825 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Overweight
Item
over-weighted
boolean
C0497406 (UMLS CUI [1])
Hypertensive disease | Diabetes Mellitus | Cardiovascular Disease | Kidney Disease | Cutaneous hypersensitivity Serious | Comorbidity Study Subject Participation Status At risk | Medical condition Study Subject Participation Status At risk | Exception Arthritis
Item
hypertension, or diabetes, or a history of cardiovascular disease or kidney disease, or serious skin allergy or other concurrent clinically significant illness or medical condition (other than arthritis) which, in the viewpoint of the study doctor, may put the subject at a possible risk for participation
boolean
C0020538 (UMLS CUI [1])
C0011849 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
C0585186 (UMLS CUI [5,1])
C0205404 (UMLS CUI [5,2])
C0009488 (UMLS CUI [6,1])
C2348568 (UMLS CUI [6,2])
C1444641 (UMLS CUI [6,3])
C3843040 (UMLS CUI [7,1])
C2348568 (UMLS CUI [7,2])
C1444641 (UMLS CUI [7,3])
C1705847 (UMLS CUI [8,1])
C0003864 (UMLS CUI [8,2])
Biological Response Modifiers | Immunosuppressive Agents
Item
patients used biologic modifier therapy or currently taking immunosuppressive agents might be excluded
boolean
C0005525 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
Therapeutic procedure Medical center Unable
Item
unable to spend 3 hours for treatment at the study center
boolean
C0087111 (UMLS CUI [1,1])
C0565990 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial