ID

40931

Description

A Clinical Trial Evaluating Platelet Rich Plasma Versus Hyaluronic-Acid in the Short-term Treatment of Symptomatic OA (Osteoarthritis) of the Hip; ODM derived from: https://clinicaltrials.gov/show/NCT01920152

Link

https://clinicaltrials.gov/show/NCT01920152

Keywords

  1. 6/7/20 6/7/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 7, 2020

DOI

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License

Creative Commons BY 4.0

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Eligibility Hip Osteoarthritis NCT01920152

Eligibility Hip Osteoarthritis NCT01920152

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female age 40-72 inclusive.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
symptomatic early oa of the hip (kellgren-lawrence grade 1-2) documented by x-ray taken within the past 6 months.
Description

Hip osteoarthritis (early-onset) Symptomatic Kellgren-Lawrence score | X-Ray Computed Tomography

Data type

boolean

Alias
UMLS CUI [1,1]
C1851543
UMLS CUI [1,2]
C0231220
UMLS CUI [1,3]
C3177117
UMLS CUI [2]
C0040405
women of childbearing potential will be allowed to enroll but must be willing to practice one highly effective method of contraception (oral, injectable or implanted hormonal methods of contraception, placement of an intrauterine device (iud) or intrauterine system (ius) condom or occlusive cap with spermicidal foam/gel/film/cream/suppository, male sterilization, or true abstinence) throughout the study.
Description

Childbearing Potential Contraceptive methods Quantity | Oral contraception | Injectable contraception | Contraceptive implant Hormonal | Intrauterine Devices | Intrauterine System | Female Condoms | CERVICAL CAP FOR CONTRACEPTIVE USE | Spermicidal foam/jelly/cream/film/suppository | Male sterilization | Sexual Abstinence

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C1265611
UMLS CUI [2]
C0029151
UMLS CUI [3]
C1262153
UMLS CUI [4,1]
C1657106
UMLS CUI [4,2]
C0458083
UMLS CUI [5]
C0021900
UMLS CUI [6]
C4293370
UMLS CUI [7]
C0221829
UMLS CUI [8]
C0493327
UMLS CUI [9]
C3843415
UMLS CUI [10]
C0024559
UMLS CUI [11]
C0036899
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with polyarticular disease.
Description

POLYARTICULAR JOINT DISEASE

Data type

boolean

Alias
UMLS CUI [1]
C0747730
patients with major conditions such as poorly control diabetes, cardiac heart failure (chf), chronic obstructive pulmonary disease (copd) or untreated depression
Description

Condition Major | Poorly controlled diabetes mellitus | Heart failure | Chronic Obstructive Airway Disease | Depressive disorder Untreated

Data type

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0205164
UMLS CUI [2]
C0554876
UMLS CUI [3]
C0018801
UMLS CUI [4]
C0024117
UMLS CUI [5,1]
C0011581
UMLS CUI [5,2]
C0332155
patients with blood disorders (blood disorders (thrombopathy, thrombocytopenia, anemia with hemoglobin <9g/dl). only those patients with a positive history of blood disorders will have a cell blood count (cbc) performed a week prior to inclusion in the study.
Description

Hematological Disease | Thrombopathy | Thrombocytopenia | Anemia | Hemoglobin measurement | Blood Cell Count

Data type

boolean

Alias
UMLS CUI [1]
C0018939
UMLS CUI [2]
C0865262
UMLS CUI [3]
C0040034
UMLS CUI [4]
C0002871
UMLS CUI [5]
C0518015
UMLS CUI [6]
C0005771
patients who had intra-articular treatment with steroids within 3 months of randomization in this study or received more than 3 previous intra-articular steroid injections to the effected hip.
Description

Intraarticular injection of corticosteroids Recent | Intraarticular injection of corticosteroids Quantity Hip Affected

Data type

boolean

Alias
UMLS CUI [1,1]
C2064783
UMLS CUI [1,2]
C0332185
UMLS CUI [2,1]
C2064783
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0019552
UMLS CUI [2,4]
C0392760
patients who are pregnant or nursing at the time of consent.
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients with inflammatory arthritic conditions (e.g. rheumatoid arthritis)
Description

Arthritis | Rheumatoid Arthritis

Data type

boolean

Alias
UMLS CUI [1]
C0003864
UMLS CUI [2]
C0003873
non-english speaking patients. (scores used for evaluation have not been validated in spanish)
Description

Lacking Able to speak English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0564215
UMLS CUI [1,3]
C0376245
patients who had previous hip surgery
Description

Hip surgery Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C0596706
UMLS CUI [1,2]
C0205156
additional disabilities in any of the lower limbs that would interfere with any of the clinical assessments.
Description

Disability of lower limb Additional | Disability of lower limb Interferes with Clinical assessment

Data type

boolean

Alias
UMLS CUI [1,1]
C1997550
UMLS CUI [1,2]
C1524062
UMLS CUI [2,1]
C1997550
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C4534461
chronic use of nsaid (defined as taking nsaid regularly every week for the last 6 months), steroids or chemotherapy drugs
Description

NSAID chronic | Steroids chronic | Antineoplastic Agents chronic

Data type

boolean

Alias
UMLS CUI [1,1]
C0003211
UMLS CUI [1,2]
C0205191
UMLS CUI [2,1]
C0038317
UMLS CUI [2,2]
C0205191
UMLS CUI [3,1]
C0003392
UMLS CUI [3,2]
C0205191
treatment with nsaids within 15 days prior to randomization in this study
Description

Non-steroidal anti-inflammatory agent therapy

Data type

boolean

Alias
UMLS CUI [1]
C4076159
patients with a bmi over 30. due to the fact that this study utilize an injection technique which may be inaccurate in obese subjects.
Description

Body mass index

Data type

boolean

Alias
UMLS CUI [1]
C1305855

Similar models

Eligibility Hip Osteoarthritis NCT01920152

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male or female age 40-72 inclusive.
boolean
C0001779 (UMLS CUI [1])
Hip osteoarthritis (early-onset) Symptomatic Kellgren-Lawrence score | X-Ray Computed Tomography
Item
symptomatic early oa of the hip (kellgren-lawrence grade 1-2) documented by x-ray taken within the past 6 months.
boolean
C1851543 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C3177117 (UMLS CUI [1,3])
C0040405 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Quantity | Oral contraception | Injectable contraception | Contraceptive implant Hormonal | Intrauterine Devices | Intrauterine System | Female Condoms | CERVICAL CAP FOR CONTRACEPTIVE USE | Spermicidal foam/jelly/cream/film/suppository | Male sterilization | Sexual Abstinence
Item
women of childbearing potential will be allowed to enroll but must be willing to practice one highly effective method of contraception (oral, injectable or implanted hormonal methods of contraception, placement of an intrauterine device (iud) or intrauterine system (ius) condom or occlusive cap with spermicidal foam/gel/film/cream/suppository, male sterilization, or true abstinence) throughout the study.
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0029151 (UMLS CUI [2])
C1262153 (UMLS CUI [3])
C1657106 (UMLS CUI [4,1])
C0458083 (UMLS CUI [4,2])
C0021900 (UMLS CUI [5])
C4293370 (UMLS CUI [6])
C0221829 (UMLS CUI [7])
C0493327 (UMLS CUI [8])
C3843415 (UMLS CUI [9])
C0024559 (UMLS CUI [10])
C0036899 (UMLS CUI [11])
Item Group
C0680251 (UMLS CUI)
POLYARTICULAR JOINT DISEASE
Item
patients with polyarticular disease.
boolean
C0747730 (UMLS CUI [1])
Condition Major | Poorly controlled diabetes mellitus | Heart failure | Chronic Obstructive Airway Disease | Depressive disorder Untreated
Item
patients with major conditions such as poorly control diabetes, cardiac heart failure (chf), chronic obstructive pulmonary disease (copd) or untreated depression
boolean
C0348080 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0554876 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
C0024117 (UMLS CUI [4])
C0011581 (UMLS CUI [5,1])
C0332155 (UMLS CUI [5,2])
Hematological Disease | Thrombopathy | Thrombocytopenia | Anemia | Hemoglobin measurement | Blood Cell Count
Item
patients with blood disorders (blood disorders (thrombopathy, thrombocytopenia, anemia with hemoglobin <9g/dl). only those patients with a positive history of blood disorders will have a cell blood count (cbc) performed a week prior to inclusion in the study.
boolean
C0018939 (UMLS CUI [1])
C0865262 (UMLS CUI [2])
C0040034 (UMLS CUI [3])
C0002871 (UMLS CUI [4])
C0518015 (UMLS CUI [5])
C0005771 (UMLS CUI [6])
Intraarticular injection of corticosteroids Recent | Intraarticular injection of corticosteroids Quantity Hip Affected
Item
patients who had intra-articular treatment with steroids within 3 months of randomization in this study or received more than 3 previous intra-articular steroid injections to the effected hip.
boolean
C2064783 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
C2064783 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0019552 (UMLS CUI [2,3])
C0392760 (UMLS CUI [2,4])
Pregnancy | Breast Feeding
Item
patients who are pregnant or nursing at the time of consent.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Arthritis | Rheumatoid Arthritis
Item
patients with inflammatory arthritic conditions (e.g. rheumatoid arthritis)
boolean
C0003864 (UMLS CUI [1])
C0003873 (UMLS CUI [2])
Lacking Able to speak English Language
Item
non-english speaking patients. (scores used for evaluation have not been validated in spanish)
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
Hip surgery Previous
Item
patients who had previous hip surgery
boolean
C0596706 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Disability of lower limb Additional | Disability of lower limb Interferes with Clinical assessment
Item
additional disabilities in any of the lower limbs that would interfere with any of the clinical assessments.
boolean
C1997550 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C1997550 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C4534461 (UMLS CUI [2,3])
NSAID chronic | Steroids chronic | Antineoplastic Agents chronic
Item
chronic use of nsaid (defined as taking nsaid regularly every week for the last 6 months), steroids or chemotherapy drugs
boolean
C0003211 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0038317 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0003392 (UMLS CUI [3,1])
C0205191 (UMLS CUI [3,2])
Non-steroidal anti-inflammatory agent therapy
Item
treatment with nsaids within 15 days prior to randomization in this study
boolean
C4076159 (UMLS CUI [1])
Body mass index
Item
patients with a bmi over 30. due to the fact that this study utilize an injection technique which may be inaccurate in obese subjects.
boolean
C1305855 (UMLS CUI [1])

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