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Keywords
Appetite Depressants ×
- 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)
- Vital Signs (1)
- Meals (1)
- Nutritionists (1)
- Concomitant Medication (1)
- End of Study (1)
- Cotinine (1)
- Diagnostic Imaging (1)
- Ethanol (1)
- Eligibility Determination (1)
- Laboratories (1)
- Magnetic Resonance Imaging (1)
- Menstrual Cycle (1)
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29 Search results.
Itemgroups: Administrative Data, MRI Scan (Structural), fMRI
Itemgroups: 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
Itemgroups: Administrative Data, Appetite VAS, Distress VAS
Itemgroups: Administrative Data, Consent for Pharmacogenetic Research, Pharmacogenetic sampling, Withdrawal of consent for pharmacogenetic research, Sample Destruction
Itemgroup: Serology - HIV Screen
Itemgroups: Administrative Data, Non-Serious Adverse Events
Itemgroups: Administrative Data, Concomitant Medications
Itemgroups: 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
Itemgroups: Administrative Data, Liver Events Assessment, Status of Treatment Blind, Pregnancy Information, Study Conclusion, Investigator Comment Log, Investigator's signature
Itemgroups: Administrative Data, Pharmacodynamics - Blood, Pharmacokinetics - Blood
Itemgroups: 12-lead ECG Abnormalities, 12-Lead ECG Abnormalities: A. Rhythm, 12-Lead ECG Abnormalities: B. P-Wave and QRS Morphology, 12-Lead ECG Abnormalities: C. Conduction, 12-Lead ECG Abnormalities: D. Myocardial Infarction, 12-Lead ECG Abnormalities: E. Depolarisation/Repolarisation (QRS-T), 12-Lead ECG Abnormalities: Other Abnormalities
Itemgroups: Administrative Data, 12-Lead ECG