Inclusion Clinical Trials, Randomized
Item
original inclusion criteria for participation in the rcts at all sites included:
boolean
C1512693 (UMLS CUI [1,1])
C0206034 (UMLS CUI [1,2])
Indication General Anesthesia | Indication Exercise
Item
candidate for general anesthesia or unsupervised exercise.
boolean
C3146298 (UMLS CUI [1,1])
C0002915 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0015259 (UMLS CUI [2,2])
Age
Item
age ≥20 and ≤65 years.
boolean
C0001779 (UMLS CUI [1])
Body mass index
Item
body mass index >27 and ≤45 kg/m2.
boolean
C1305855 (UMLS CUI [1])
Diabetes Mellitus, Non-Insulin-Dependent Requirement Antidiabetics | Blood glucose increased | Glycosylated hemoglobin A | Plasma fasting glucose measurement | Oral Glucose Tolerance Test
Item
diagnosis of type 2 diabetes confirmed by either requiring diabetes medication and/or having elevated glycemia based on hba1c, fasting plasma glucose, and/or oral glucose tolerance test (ogtt) results, according to american diabetes association criteria.
boolean
C0011860 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0935929 (UMLS CUI [1,3])
C0595877 (UMLS CUI [2])
C0019018 (UMLS CUI [3])
C0583513 (UMLS CUI [4])
C0029161 (UMLS CUI [5])
Study Subject Participation Status Ability Willing
Item
ability and willingness to participate in the study and agree to any of the research arms.
boolean
C2348568 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Compliance behavior Study Protocol
Item
able to understand the options and to comply with the requirements of each program.
boolean
C1321605 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Childbearing Potential Urine pregnancy test negative Before Operative Surgical Procedures
Item
negative urine pregnancy test at screening and baseline visits (prior to surgery) for women of childbearing potential (i.e., biologically capable of becoming pregnant).
boolean
C3831118 (UMLS CUI [1,1])
C0430057 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0543467 (UMLS CUI [1,4])
Subject is Randomized Clinical Trials, Randomized | Intervention Initiation Never
Item
subjects who were randomized in one of the four rcts but never initiated intervention
boolean
C3815594 (UMLS CUI [1,1])
C0206034 (UMLS CUI [1,2])
C1948041 (UMLS CUI [2,1])
C1704686 (UMLS CUI [2,2])
C2003901 (UMLS CUI [2,3])
Randomization Therapeutic procedure Lacking
Item
/ did not receive randomized treatment
boolean
C0034656 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Informed Consent Refused
Item
refusal to sign informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])