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- Clinical Trial (38)
- Gynecology (38)
- Premature Birth (32)
- Electrocardiogram (ECG) (6)
- Vital Signs (5)
- Clinical Chemistry Tests (4)
- Clinical Laboratory Services (4)
- Hematology (4)
- Urinalysis (3)
- Breast Neoplasms (3)
- End of Study (3)
- Pharmacogenetics (2)
- Pharmacokinetics (2)
- Adverse event (2)
- Concomitant Medication (2)
- Drug trial (2)
- Death (2)
- Eligibility Determination (2)
- Psychology, Clinical (1)
- Questionnaires (1)
- Random Allocation (1)
- Social Sciences (1)
- Cognitive Therapy (1)
- Patient Selection (1)
- Depression, Postpartum (1)
- Brain Neoplasms (1)
- Treatment Form (1)
- Trial screening (1)
- Demography (1)
- Double-Blind Method (1)
- Follow-Up Studies (1)
- Medical Oncology (1)
- Neoplasm Metastasis (1)
- Office Visits (1)
- Ovarian Neoplasms (1)
- Pathology (1)
- Patient Admission (1)
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Modèles de données sélectionnés
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39 Résultats de recherche.
Groupes Item: Date of visit, Vital signs, 12 lead ECG, 12 lead ECG, Abnormality, Experimental drug, Continuation status, Laboratory Procedures, Chemistry, Clinical, Laboratory Procedures, Hematology finding, Conclusion, Clinical Research, Cessation of life, Pregnancy, Information
Groupes Item: Date of visit, Assessment Date, Cessation of life, Pregnancy, Information, Conclusion, Clinical Research
Groupes Item: Header Module, Header Module, Header, Tests & Procedures Relevant to Pregnancy, Pregnancy Information, Pregnancy Status/Pregnancy Outcome, Fetal/Baby Outcome, Footer Module
Groupes Item: 12 lead ECG, Dosage, Date in time, Time, 12 lead ECG, Pre-dose, 12 lead ECG, Post-dose, 30 Minutes, 12 lead ECG, Post-dose, 1 Hour, 12 lead ECG, 2 hours post-dose, 12 lead ECG, 4 hours post-dose, 12 lead ECG, Post-dose, 8 Hours, 12 lead ECG, Post-dose, 12 Hours, 12 lead ECG, Post-dose, 24 Hours
Groupe Item: Pregnancy, Information
Groupes Item: Inclusion Criteria, Exclusion Criteria
Groupes Item: Experimental drug, Dosage, Rapid, Experimental drug, Dosing, Continuous, Betamethasone, Dosage
Groupe Item: Pharmacogenetic Test, Informed Consent, Withdraw
Groupe Item: Pharmacogenetic Test, Informed Consent
Groupe Item: 12 lead ECG, Abnormality
Groupe Item: 12 lead ECG
Groupe Item: Concomitant Agent