| OutcomeVariable: Nonfatal myocardial infarction or stroke | 
      
        
          | OutcomeVariable: Remission of diabetes | 
      
        
          | OutcomeVariable: New onset depression | 
      
        
          | OutcomeVariable_Treatment_with_opioids | 
      
        
          | OutcomeVariable_Additional_GI_surgical_procedure | 
      
        
          | OutcomeVariable: HbA1c at 12 months | 
      
        
          | OutcomeVariable: HbA1c at 36 months | 
      
        
          | OutcomeVariable: HbA1c at 24 months | 
      
        
          | OutcomeVariable: HbA1c at 60 months | 
      
        
          | OutcomeVariable: HbA1c at 6 months | 
      
        
          | ExposureVariable: Age (as continuous variable) | 
      
        
          | ExposureVariable: Body Mass Index (as continuous variable) | 
      
        
          | ExposureVariable: pht013093.v1.p1 SUBJECT_ID | 
      
        
          | ExposureVariable: pht013093.v1.p1 SEX | 
      
        
          | ExposureVariable: pht013093.v1.p1 RACE | 
      
        
          | ExposureVariable: pht013093.v1.p1 Age at diagnosis | 
      
        
          | ExposureVariable: pht013094.v1.p1 SAMPLE_ID | 
      
        
          | ExposureVariable: pht013094.v1.p1 BODY_SITE | 
      
        
          | ExposureVariable: pht013094.v1.p1 SAMPLE_USE | 
      
        
          | ExposureVariable: pht013094.v1.p1 ANALYTE_TYPE | 
      
        
          | ExposureVariable: pht013094.v1.p1 Source_Type | 
      
        
          | ExposureVariable: pht013094.v1.p1 IS_TUMOR | 
      
        
          | Percentage of Participants Achieving Treatment Success During Controlled Insulin-Induced Hypoglycemia (NCT03421379) | 
      
        
          | Pharmacodynamics (PD): Change From Baseline in Maximal Blood Glucose (BGmax) of Glucagon Nasal Powder and Glucagon Hydrochloride Intramuscular (IM) (NCT03421379) | 
      
        
          | PD: Time to Maximal Concentration (Tmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) | 
      
        
          | Pharmacokinetics (PK): Change From Baseline in Area Under the Concentration Versus Time Curve From Zero to Time t (AUC [0-tLast]) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) | 
      
        
          | PK: Change From Baseline in Maximal Concentration (Cmax) of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) | 
      
        
          | PK: Change From Baseline in Tmax of Glucagon Nasal Powder and Glucagon Hydrochloride IM (NCT03421379) | 
      
        
          | NHANES SEQN Respondent Sequence Number | 
      
        
          | NHANES LBXGLU: Fasting Glucose (mg/dL) | 
      
        
          | NHANES LBDGLUSI: Fasting Glucose (mmol/L) | 
      
        
          | NHANES WTSAF2YR: Fasting Subsample 2 Year MEC Weight | 
      
        
          | Median Age of Parachute Intervention Group | 
      
        
          | Age | 
      
        
          | Sex | 
      
        
          | Ethnic Group | 
      
        
          | Height | 
      
        
          | History of Broken Bones | 
      
        
          | History of Acrophobia | 
      
        
          | History of Parachute Use | 
      
        
          | Family History of Parachute Use | 
      
        
          | Frequent Flier | 
      
        
          | International vs Domestic Flight | 
      
        
          | Aircraft Type | 
      
        
          | Velocity | 
      
        
          | Altitude | 
      
        
          | Outcome: Death or Major Traumatic Injury on Impact | 
      
        
          | Outcome: Injury Severity Score on Impact | 
      
        
          | Outcome: Death or Major Traumatic Injury 30 days after Impact | 
      
        
          | Outcome: Injury Severity Score 30 days after Impact | 
      
        
          | Health Survey Score Total | 
      
        
          | Health Survey Score-Physical Health Subscore | 
      
        
          | Health Survey Score-Mental Health Subscore | 
      
        
          | Weight | 
      
        
          | OutcomeVariable: American Diabetes Association composite triple end point for metabolic control at 5 years | 
      
        
          | VariableDefinition: Gender | 
      
        
          | VariableDefinition: Condition(s) | 
      
        
          | VariableDefinition: Comparator | 
      
        
          | VariableDefinition: Unit | 
      
        
          | VariableDefinition: NTproBNP | 
      
        
          | VariableDefinition: Date of birth | 
      
        
          | VariableDefinition: Date of measurement | 
      
        
          | EvidenceVariable: Time of measurement | 
      
        
          | Time to integration of results in a recommendation | 
      
        
          | EvidenceVariable: Patient id | 
      
        
          | EvidenceVariable: case_id | 
      
        
          | Change in Mean Systolic Blood Pressure (NCT03640312) | 
      
        
          | Mean Systolic Blood Pressure (NCT03640312) | 
      
        
          | Change in Mean Diastolic Blood Pressure (NCT03640312) | 
      
        
          | Mean Diastolic Blood Pressure (NCT03640312) | 
      
        
          | Proportion of Patients With Hypertension Control (NCT03640312) | 
      
        
          | Number of Patients Requiring Step up Treatment (NCT03640312) | 
      
        
          | Proportion of Patients With Adverse Event Free Hypertension Control (NCT03640312) | 
      
        
          | Medication Adherence (NCT03640312) | 
      
        
          | Health-related Quality of Life (NCT03640312) | 
      
        
          | Change in Mean Systolic Blood Pressure (NCT03640312) | 
      
        
          | Percentage of Participants With Serious Adverse Events (SAEs) (NCT03640312) | 
      
        
          | Percentage of Participants With Potentially Related Adverse Events (NCT03640312) | 
      
        
          | Rate of Adverse Events of Special Interest (NCT03640312) | 
      
        
          | Mean Change in Serum Potassium (NCT03640312) | 
      
        
          | Mean Change in Serum Sodium (NCT03640312) | 
      
        
          | Mean Change in Blood Urea Nitrogen (NCT03640312) | 
      
        
          | Mean Change in Serum Creatinine (NCT03640312) | 
      
        
          | Proportion of Patients With Hypertension Control at 6 and 12 weeks - 6 weeks at  (NCT03640312) | 
      
        
          | Proportion of Patients With Hypertension Control at 6 and 12 weeks - 12 weeks at  (NCT03640312) | 
      
        
          | Health-related Quality of Life at 12 weeks - Change in Physical Health T score (PROMIS) at  (NCT03640312) | 
      
        
          | Health-related Quality of Life at 12 weeks - Change in Mental Health T score (PROMIS) at  (NCT03640312) | 
      
        
          | Systolic blood pressure at 12 weeks | 
      
        
          | Diastolic blood pressure at 12 weeks | 
      
        
          | Medication Adherence at 12 weeks | 
      
        
          | Hypertension Control at 12 weeks | 
      
        
          | Add-on Amlodipine at 6 weeks | 
      
        
          | Adverse event free and hypertension control at 12 weeks | 
      
        
          | OutcomeVariable: Mean difference in HbA1c between Surgery and Medical/Lifestyle groups at end of follow-up | 
      
        
          | OutcomeVariable_All_cause_mortality |