Informatie:
Fout:
Trefwoorden
GLIUKOKORTIKOIDOV ANALOGI ×
- Clinical Trial (63)
- Rhinitis, Allergic, Perennial (27)
- Healthy Volunteers (27)
- Drug trial (23)
- Pulmonary Disease, Chronic Obstructive (22)
- Asthma (7)
- Adverse event (7)
- Electrocardiogram (ECG) (6)
- On-Study Form (5)
- Liver (5)
- Biopsy (4)
- Vital Signs (4)
- Concomitant Medication (3)
- Trial screening (3)
- End of Study (3)
- Diagnostic Imaging (3)
- Pneumonia (2)
- Pregnancy (2)
- Pregnancy Tests (2)
- Blood (2)
- Disease Progression (2)
- Fractures, Bone (2)
- Administration, Inhalation (2)
- Meals (2)
- Pharmacogenetics (1)
- Pharmacokinetics (1)
- Physical Examination (1)
- Research Personnel (1)
- Respiratory Function Tests (1)
- Serology (1)
- Substance Abuse Detection (1)
- Urinalysis (1)
- Clinical Chemistry Tests (1)
- Urine Specimen Collection (1)
- Tobacco Use (1)
- Treatment Form (1)
- Compliance (1)
- Cotinine (1)
- Demography (1)
- Alcohol Drinking (1)
- Drug Evaluation (1)
- Eligibility Determination (1)
- Equipment and Supplies (1)
- Equipment Failure (1)
- Follow-Up Studies (1)
- Hepatitis B (1)
- Hepatitis C (1)
- HIV (1)
- Information Systems (1)
- Informed Consent (1)
- Laboratories (1)
- Liver Diseases (1)
Inhoudsopgave
Geselecteerde datamodellen
U moet ingelogd zijn om meerdere datamodellen te selecteren en die te downloaden of te analyseren.
63 Zoekresultaten.
Itemgroep: Pneumonia Assessment
Itemgroep: Pneumonia Assessment
Itemgroep: Liver Biopsy
Itemgroep: Chest X-Ray
Itemgroepen: COPD exacerbations, Contact Method/Treatment Site for Exacerbations, Exacerbation Medications
Itemgroep: LOG Status
Itemgroepen: Subject withdrawal, Pre-Dose Vital Signs, Candidiasis examination, Electronically transferred lab data, Liver Events Assessment, Smoking Status
Itemgroepen: Subject withdrawal, Pre-Dose Vital Signs, Candidiasis examination, Electronically transferred lab data, Liver Events Assessment, Smoking Status
Itemgroepen: Randomisation, Pre-Dose Vital Signs, Candidiasis examination, Electronically transferred lab data, Liver Events Assessment, Smoking Status, Subject withdrawal
Itemgroepen: Serious Adverse Event, Intensity Changes, concomitant medication, Relevant medical conditions/Risk factors, Relevant Diagnostic Results, Rechallenge, Investigational product
Itemgroepen: Demography, Eligibility Question, Previous clinical trial participation, Vital Signs, Disease Duration, Medical conditions, Exacerbation History, History of Tobacco Use, Oropharyngeal candidiasis examination, Chest X-Ray, Electronically transferred lab data, Rescreening of subject
Itemgroep: Investigational Product Compliance