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ID
35719
Beschrijving
Placement of Hydrophilic TiZr Implants in Diabetic Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02395315
Link
https://clinicaltrials.gov/show/NCT02395315
Trefwoorden
Versies (1)
- 18-03-19 18-03-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
18 maart 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Diabetes Mellitus NCT02395315
Eligibility Diabetes Mellitus NCT02395315
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes Mellitus NCT02395315
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Adult | Diabetes Mellitus, Non-Insulin-Dependent | Partially edentulous mandible
Item
1. adult patients with diagnosed type ii dm exhibiting at least one edentulous site in the posterior mandible.
boolean
C0001675 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C1299631 (UMLS CUI [3])
C0011860 (UMLS CUI [2])
C1299631 (UMLS CUI [3])
History of diabetes mellitus Duration
Item
2. history of diabetes for at least two years prior to enrollment.
boolean
C0455488 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Hemoglobin A1c measurement Group Poorly controlled | Hemoglobin A1c measurement Group Well controlled
Item
3. hba1c >7.5% & <10% for enrollment in the pc group and hba1c ≤ 7.0% for enrollment in the wc group.
boolean
C0474680 (UMLS CUI [1,1])
C0441833 (UMLS CUI [1,2])
C3853134 (UMLS CUI [1,3])
C0474680 (UMLS CUI [2,1])
C0441833 (UMLS CUI [2,2])
C3853142 (UMLS CUI [2,3])
C0441833 (UMLS CUI [1,2])
C3853134 (UMLS CUI [1,3])
C0474680 (UMLS CUI [2,1])
C0441833 (UMLS CUI [2,2])
C3853142 (UMLS CUI [2,3])
Pregnancy | Breast Feeding | Pregnancy, Planned | Gender Pregnancy Test
Item
1. females during pregnancy or lactation and females that plan to become pregnant in the following year (pregnancy test will be provided prior to enrollment).
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0079399 (UMLS CUI [4,1])
C0032976 (UMLS CUI [4,2])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0079399 (UMLS CUI [4,1])
C0032976 (UMLS CUI [4,2])
Other Coding | Alveolar Bone Loss
Item
2. mandibular incisor sites that will not allow bone core retrieval due to limited alveolar bone width.
boolean
C3846158 (UMLS CUI [1])
C0002382 (UMLS CUI [2])
C0002382 (UMLS CUI [2])
Tobacco use
Item
3. smokers.
boolean
C0543414 (UMLS CUI [1])
Pharmaceutical Preparations Affecting Bone healing | Diphosphonates | Steroids chronic
Item
4. medications that affect bone healing (e.g. bisphosphonates or chronic steroids)
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C1321023 (UMLS CUI [1,3])
C0012544 (UMLS CUI [2])
C0038317 (UMLS CUI [3,1])
C0205191 (UMLS CUI [3,2])
C0392760 (UMLS CUI [1,2])
C1321023 (UMLS CUI [1,3])
C0012544 (UMLS CUI [2])
C0038317 (UMLS CUI [3,1])
C0205191 (UMLS CUI [3,2])
Periodontal Disease
Item
5. active periodontal disease.
boolean
C0031090 (UMLS CUI [1])
Study Subject Participation Status Unwilling | Informed Consent Unwilling
Item
6. patients that will not agree to participate in this study or sign the consent form.
boolean
C2348568 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Carrier Communicable Diseases
Item
7. patients who are carriers of transmissible disease(s) that may unnecessarily expose laboratory personnel to risks.
boolean
C0560175 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
C0009450 (UMLS CUI [1,2])
Osteoporosis Z-score
Item
8. participants with a physician-diagnosed osteoporosis (z-score ≤ -2).
boolean
C0029456 (UMLS CUI [1,1])
C0871421 (UMLS CUI [1,2])
C0871421 (UMLS CUI [1,2])