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LIJEKOVI, ISTRAŽIVANJE ×
- Clinical Trial (203)
- Vital Signs (78)
- Pharmacokinetics (58)
- Laboratories (50)
- Electrocardiogram (ECG) (41)
- Clinical Trial, Phase I (40)
- Pulmonary Medicine (34)
- Medical Oncology (25)
- Pulmonary Disease, Chronic Obstructive (24)
- Anxiety Disorders (22)
- Paroxetine (21)
- Depressive Disorder (21)
- Pharmaceutical Preparations (21)
- Hematology (21)
- Respiratory Function Tests (20)
- Neurology (20)
- Asthma (19)
- Adverse event (19)
- Treatment Form (19)
- Diabetes Mellitus, Type 2 (17)
- Testosterone (14)
- Hypogonadism (14)
- Migraine Disorders (14)
- Sumatriptan (13)
- On-Study Form (13)
- Liver (13)
- Peritoneal Neoplasms (12)
- Cross-Over Studies (12)
- Clinical Chemistry Tests (12)
- Fallopian Tube Neoplasms (12)
- Gynecology (12)
- Hypertension (12)
- Ovarian Neoplasms (12)
- Pharmacogenetics (11)
- Consent Forms (11)
- Therapeutics (10)
- Concomitant Medication (10)
- Non Small Cell Lung Cancer (10)
- Parkinsons Disease (10)
- Disease (10)
- Urinalysis (9)
- Hypereosinophilic Syndrome (9)
- Contraceptives, Oral, Combined (9)
- Telemetry (8)
- Blood (8)
- Blood Pressure (8)
- Drug trial (8)
- Compliance (8)
- Random Allocation (7)
- Clinical Trial, Phase III (7)
- Type 2 Diabetes (7)
- Double-Blind Method (7)
- Placebos (6)
- Arthritis, Rheumatoid (6)
- Restless Legs Syndrome (6)
- Thyroid Hormones (6)
- Randomized Controlled Trial (6)
- Blood Glucose (6)
- Alcohol Drinking (6)
- Eligibility Determination (6)
- Glucose Tolerance Test (6)
- Medical Records (6)
- Pregnancy (5)
- Arthritis (5)
- Rheumatology (5)
- Biopsy (5)
- Diagnostic Imaging (5)
- Drug Administration Schedule (5)
- Eye Diseases (5)
- Macular Degeneration (5)
- Psychiatry (4)
- Risk Factors (4)
- Urine (4)
- Biological Markers (4)
- Premature Ejaculation (4)
- Drug-Related Side Effects and Adverse Reactions (4)
- Physical Examination (3)
- Atherosclerosis (3)
- Healthy Volunteers (3)
- End of Study (3)
- Alzheimer Disease (3)
- Pregnancy Tests (2)
- Rhinitis (2)
- Schizophrenia (2)
- Steroids (2)
- Bacterial Infections (2)
- Vaccines (2)
- Purpura, Thrombocytopenic, Idiopathic (2)
- Clinical Trial, Phase IV (2)
- Blood Specimen Collection (2)
- Body Temperature (2)
- Substance-Related Disorders (2)
- Measles-Mumps-Rubella Vaccine (2)
- Child (2)
- Adrenergic beta-2 Receptor Agonists (2)
- Transcriptome (2)
- Meals (2)
- Death (2)
- Demography (2)
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224 Resultados de la búsqueda.
Itemgroup: General Information
Itemgroups: Administrative data, Pregnancy Notification Form (Subject), Mother's Relevant Medical/Family History, If applicable, record the number in the appropriate categories below:, Father's Relevant Medical/Family History, Drug Exposures, Reporting Investigator Information
Itemgroups: Administrative data, Adverse Events
Itemgroups: Administrative data, Concomitant Medications
Itemgroups: Administrative data, Investigational Product - Regimen A - 40 mg Carvedilol CR, Investigational Product - 40 mg Carvedilol Regimen B Alcohol Ingestion - 240 ml OF 20%EtOH, Investigational Product - Regimen C Alcohol Ingestion - 240 ml OF 20% EtOH, Investigational Product - Regimen D Alcohol Ingestion - 240 ml OF 20% EtOH
Itemgroups: Administrative data, Investigational Product - Regimen A - 40 mg Carvedilol CR, Investigational Product - 40 mg Carvedilol Regimen B Alcohol Ingestion - 240 ml OF 20%EtOH, Investigational Product - Regimen C Alcohol Ingestion - 240 ml OF 20% EtOH, Investigational Product - Regimen D Alcohol Ingestion - 240 ml OF 20% EtOH
Itemgroups: Administrative data, Regimen
Itemgroups: Administrative data, Regimen
Itemgroups: Administrative data, Investigational Product - Regimen A - 40 mg Carvedilol CR, Investigational Product - 40 mg Carvedilol Regimen B Alcohol Ingestion - 240 ml OF 20%EtOH, Investigational Product - Regimen C Alcohol Ingestion - 240 ml OF 20% EtOH, Investigational Product - Regimen D Alcohol Ingestion - 240 ml OF 20% EtOH
Itemgroups: Administrative data, Regimen
Itemgroups: Administrative data, Investigational Product - Regimen A - 40 mg Carvedilol CR, Investigational Product - 40 mg Carvedilol Regimen B Alcohol Ingestion - 240 ml OF 20%EtOH, Investigational Product - Regimen C Alcohol Ingestion - 240 ml OF 20% EtOH, Investigational Product - Regimen D Alcohol Ingestion - 240 ml OF 20% EtOH
Itemgroups: Administrative data, Serious Adverse Event (SAE), Section 1, Section 2 - Seriousness, Section 3 - Demography Data, Section 4, Section 5 - Possible Causes of SAE, Section 6 - Relevant Medical Conditions, Section 7 - Relevant Risk Factors, Section 8 - Relevant Concomitant Medications, Section 9 - Investigational Product, Section 10 - Relevant Assessment, Section 11 - Narrative Remarks, Administrative data