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- Clinical Trial (29)
- Obesity (29)
- Questionnaires (3)
- Adverse event (3)
- Liver (3)
- Electrocardiography, Ambulatory (2)
- Trial screening (2)
- Electrocardiogram (ECG) (2)
- Appetite (1)
- Pharmacogenetics (1)
- Pharmacology (1)
- Physical Examination (1)
- Pregnancy (1)
- Pregnancy Tests (1)
- Random Allocation (1)
- Serology (1)
- Stress, Psychological (1)
- Telemetry (1)
- Substance Abuse Detection (1)
- Biopsy (1)
- Body Weight (1)
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- Meals (1)
- Nutritionists (1)
- Concomitant Medication (1)
- End of Study (1)
- Cotinine (1)
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- Ethanol (1)
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29 Zoekresultaten.
Itemgroepen: Administrative Data, Alcohol Breath Test, Cotinine Screen, Drug Screen
Itemgroepen: Administrative Data, Questionnaires at Screening
Itemgroepen: Administrative Data, Pre-Dose and 2h post-Dose Questionnaires, 4 and 10 h post-Dose Questionnaire, 5, (8), 24 hrs post-Dose questionnaires
Itemgroepen: Administrative Data, Laboratory Data
Itemgroepen: Administrative Data, Non-Serious Adverse Events
Itemgroepen: Administrative Data, Mother's relevant medical/family history, Father's Relevant Medical/Family History, Drug exposures, Subject withdrawal, information investigator
Itemgroepen: Administrative Data, Liver imaging, General Liver imaging results, Focal Hepatic Lesions, Gallstones or gallbladder lesions, Biliary ductal lesions, Portal/Hepatic vein abnormalities
Itemgroepen: Administrative Data, Liver Chemistry Result at/above Investigational Product stopping Criteria, Start and End Date of Investigational Product, Subject Factors, Diagnostics Liver Event, Unscheduled PK blood sample, Specific Medical Conditions at onset of liver event
Itemgroepen: Administrative Data, Liver Biopsy, Final Diagnosis, Liver Architecture, Description of Liver Cells or Hepatocytes, Liver Cell or Hepatocyte Inclusions or Vacuoles, Hepatocyte or Liver Cell Nuclear Abnormalities, Liver or Lobular Infiltrates, Portal Tract Inflammation, Bile Ducts, Portal Veins, Liver Infections, Parasites or Ova, Histologic Staining or Additional Studies Obtained
Itemgroepen: Administrative Data, Serious Adverse Events - Section 1, Serious Adverse Events - Section 2: Seriousness, Serious Adverse Events - Section 3: Demography Data, Serious Adverse Events - Section 4: Recurrence, Serious Adverse Events - Section 5: Causes Of SAE Other Than Investigational Products, Serious Adverse Events - Section 6: Relevant medical conditions, Serious Adverse Events - Section 7: Other relevant risk factors, Serious Adverse Events - Section 8: Relevant concomitant medication, Serious Adverse Events - Section 9: Details of investigational Products, Serious Adverse Events - Section 10: Details of relevant assessments, Serious Adverse Events - Section 11: Narrative Remarks
Itemgroepen: Administrative Data, Concomitant Medications
Itemgroepen: Administrative Data, Liver Events Assessment, Status of Treatment Blind, Pregnancy Information, Study Conclusion, Investigator Comment Log, Investigator's signature