ID

36698

Description

Autologous Adipose-Derived Stromal Cells Delivered Intra-articularly in Patients With Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT01739504

Lien

https://clinicaltrials.gov/show/NCT01739504

Mots-clés

Versions (1)
  1. 02/06/2019 02/06/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

2 juin 2019

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 Osteoarthritis NCT01739504

Anglais

Eligibility Osteoarthritis NCT01739504

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females between age 18 and 80 years.
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
patient with current proven diagnosis of osteoarthritis, with consistent symptomatology
Description

Osteoarthritis | Symptoms Consistent with Osteoarthritis

Type de données

boolean

Alias
UMLS CUI [1]
C0029408
UMLS CUI [2,1]
C1457887
UMLS CUI [2,2]
C0332290
UMLS CUI [2,3]
C0029408
up to date on all age and gender appropriate cancer screening per american cancer society (refer to section 9.3 for more details).
Description

Screening for cancer Appropriate Age | Screening for cancer Appropriate Gender

Type de données

boolean

Alias
UMLS CUI [1,1]
C0199230
UMLS CUI [1,2]
C1548787
UMLS CUI [1,3]
C0001779
UMLS CUI [2,1]
C0199230
UMLS CUI [2,2]
C1548787
UMLS CUI [2,3]
C0079399
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
females who are pregnant or nursing or females of childbearing potential who are unwilling to maintain contraceptive therapy for the duration of the study
Description

Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Unwilling

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0700589
UMLS CUI [3,3]
C0558080
life expectancy < 6 months due to concomitant illnesses.
Description

Life Expectancy Due to Comorbidity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0009488
exposure to any investigational drug or procedure within 1 month prior to study entry or enrolled in a concurrent study that may confound results of this study.
Description

Exposure to Investigational New Drugs | Exposure to Interventional procedure | Study Subject Participation Status Interferes with Research results

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332157
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C0332157
UMLS CUI [2,2]
C0184661
UMLS CUI [3,1]
C2348568
UMLS CUI [3,2]
C0521102
UMLS CUI [3,3]
C0683954
active infectious disease. patients known to have tested positive for hiv, htlv, hbv, hcv, cmv (igm > igg) and/or syphilis will have an expert consultation as to patient eligibility based on the patient's infectious status
Description

Communicable Diseases | HIV Seropositivity | HTLV test positive | Hepatitis B virus test positive | Hepatitis C virus test positive | Cytomegalovirus test positive | Syphilis

Type de données

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0019699
UMLS CUI [3]
C1608943
UMLS CUI [4]
C2748184
UMLS CUI [5]
C2748185
UMLS CUI [6]
C0948099
UMLS CUI [7]
C0039128
any illness which, in the investigator's judgment, will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results
Description

Illness Interferes with Protocol Compliance | Illness compromises Patient safety | Illness Interferes with Interpretation Research results

Type de données

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0525058
UMLS CUI [2,1]
C0221423
UMLS CUI [2,2]
C2945640
UMLS CUI [2,3]
C1113679
UMLS CUI [3,1]
C0221423
UMLS CUI [3,2]
C0521102
UMLS CUI [3,3]
C0459471
UMLS CUI [3,4]
C0683954
patients on chronic immunosuppressive transplant therapy
Description

Immunosuppressive therapy for transplant chronic

Type de données

boolean

Alias
UMLS CUI [1,1]
C0521304
UMLS CUI [1,2]
C0205191
systolic blood pressure (supine) ≤90 mmhg or greater than 180mmhg
Description

Lying systolic blood pressure

Type de données

boolean

Alias
UMLS CUI [1]
C1319895
resting heart rate > 100 bpm;
Description

RESTING HEART RATE

Type de données

boolean

Alias
UMLS CUI [1]
C1821417
known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate.
Description

Substance Dependence Interferes with Completion of clinical trial | Substance Dependence Interferes with Interpretation Research results | Factor Interferes with Completion of clinical trial | Factor Interferes with Interpretation Research results | Study Subject Participation Status Inappropriate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0038580
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2732579
UMLS CUI [2,1]
C0038580
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0459471
UMLS CUI [2,4]
C0683954
UMLS CUI [3,1]
C1521761
UMLS CUI [3,2]
C0521102
UMLS CUI [3,3]
C2732579
UMLS CUI [4,1]
C1521761
UMLS CUI [4,2]
C0521102
UMLS CUI [4,3]
C0459471
UMLS CUI [4,4]
C0683954
UMLS CUI [5,1]
C2348568
UMLS CUI [5,2]
C1548788
history of cancer (other than non-melanoma skin cancer or in-situ cervical cancer) in the last five years.
Description

Malignant Neoplasms | Exception Skin carcinoma | Exception Carcinoma in situ of uterine cervix

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0851140
active clinical infection
Description

Communicable Disease

Type de données

boolean

Alias
UMLS CUI [1]
C0009450
unwilling and/or not able to give written informed consent.
Description

Informed Consent Unwilling | Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
Retour au début de la page

Similar models

Eligibility Osteoarthritis NCT01739504

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
males and females between age 18 and 80 years.
boolean
C0001779 (UMLS CUI [1])
Osteoarthritis | Symptoms Consistent with Osteoarthritis
Item
patient with current proven diagnosis of osteoarthritis, with consistent symptomatology
boolean
C0029408 (UMLS CUI [1])
C1457887 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0029408 (UMLS CUI [2,3])
Screening for cancer Appropriate Age | Screening for cancer Appropriate Gender
Item
up to date on all age and gender appropriate cancer screening per american cancer society (refer to section 9.3 for more details).
boolean
C0199230 (UMLS CUI [1,1])
C1548787 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,3])
C0199230 (UMLS CUI [2,1])
C1548787 (UMLS CUI [2,2])
C0079399 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding | Childbearing Potential Contraceptive methods Unwilling
Item
females who are pregnant or nursing or females of childbearing potential who are unwilling to maintain contraceptive therapy for the duration of the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0558080 (UMLS CUI [3,3])
Life Expectancy Due to Comorbidity
Item
life expectancy < 6 months due to concomitant illnesses.
boolean
C0023671 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Exposure to Investigational New Drugs | Exposure to Interventional procedure | Study Subject Participation Status Interferes with Research results
Item
exposure to any investigational drug or procedure within 1 month prior to study entry or enrolled in a concurrent study that may confound results of this study.
boolean
C0332157 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0332157 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
C2348568 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0683954 (UMLS CUI [3,3])
Communicable Diseases | HIV Seropositivity | HTLV test positive | Hepatitis B virus test positive | Hepatitis C virus test positive | Cytomegalovirus test positive | Syphilis
Item
active infectious disease. patients known to have tested positive for hiv, htlv, hbv, hcv, cmv (igm > igg) and/or syphilis will have an expert consultation as to patient eligibility based on the patient's infectious status
boolean
C0009450 (UMLS CUI [1])
C0019699 (UMLS CUI [2])
C1608943 (UMLS CUI [3])
C2748184 (UMLS CUI [4])
C2748185 (UMLS CUI [5])
C0948099 (UMLS CUI [6])
C0039128 (UMLS CUI [7])
Illness Interferes with Protocol Compliance | Illness compromises Patient safety | Illness Interferes with Interpretation Research results
Item
any illness which, in the investigator's judgment, will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results
boolean
C0221423 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0221423 (UMLS CUI [2,1])
C2945640 (UMLS CUI [2,2])
C1113679 (UMLS CUI [2,3])
C0221423 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0459471 (UMLS CUI [3,3])
C0683954 (UMLS CUI [3,4])
Immunosuppressive therapy for transplant chronic
Item
patients on chronic immunosuppressive transplant therapy
boolean
C0521304 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
Lying systolic blood pressure
Item
systolic blood pressure (supine) ≤90 mmhg or greater than 180mmhg
boolean
C1319895 (UMLS CUI [1])
RESTING HEART RATE
Item
resting heart rate > 100 bpm;
boolean
C1821417 (UMLS CUI [1])
Substance Dependence Interferes with Completion of clinical trial | Substance Dependence Interferes with Interpretation Research results | Factor Interferes with Completion of clinical trial | Factor Interferes with Interpretation Research results | Study Subject Participation Status Inappropriate
Item
known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate.
boolean
C0038580 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])
C0038580 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0459471 (UMLS CUI [2,3])
C0683954 (UMLS CUI [2,4])
C1521761 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C2732579 (UMLS CUI [3,3])
C1521761 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C0459471 (UMLS CUI [4,3])
C0683954 (UMLS CUI [4,4])
C2348568 (UMLS CUI [5,1])
C1548788 (UMLS CUI [5,2])
Malignant Neoplasms | Exception Skin carcinoma | Exception Carcinoma in situ of uterine cervix
Item
history of cancer (other than non-melanoma skin cancer or in-situ cervical cancer) in the last five years.
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0851140 (UMLS CUI [3,2])
Communicable Disease
Item
active clinical infection
boolean
C0009450 (UMLS CUI [1])
Informed Consent Unwilling | Informed Consent Unable
Item
unwilling and/or not able to give written informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
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