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- Clinical Trial (674)
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Table des matières
Modèles de données sélectionnés
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825 Résultats de recherche.
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose modification
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose reduction
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose reduction
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose reduction
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose reduction
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose reduction
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose reduction
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression
Groupes Item: Study medication record since last visit, RLS Rating Scale, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Instructions for the investigator, Clinical Global impression, Dose reduction
Groupes Item: Study entry, Vital signs, Medical Procedures, Concomitant Medication, Adverse reaction, Exclusion Criterion, Healthcare resource utilisation - visits/contacts with physician, Healthcare resource utilisation - visits/contacts with physician, Healthcare resource utilisation - Visits/Contacts with other Paramedical Practitioners, Healthcare resource utilisation - Visits/Contacts with other Paramedical Practitioners, Healthcare resource utilisation - Hospitalisation, Healthcare resource utilisation - hospitalisation, Healthcare resource utilisation - accident & emergency / emergency room visits, Healthcare resource utilisation - accident & emergency / emergency room visits, Clinical Global impression, RLS Rating scale, Patient rated scale, Pregnancy information, Study Subject Participation Status, Investigator signature, Orthostatic vital signs, Pre-Dose Reading 1, Pre-Dose Reading 2, Pre-Dose Reading 3, Time of dose, 2 hours Post-Dose Reading 1
Groupes Item: Vital signs, Laboratory Evaluation, Urine Dipstick, Pregnancy dipstick, Medical Procedures, Medical Procedures, Prior and concomitant medication, prior and concomitant medication, Baseline signs and symptoms, Significant medical/surgical history and physical examination, Significant medical/surgical history and physical examination, Study Subject Participation Status, Investigator signature, Repeated Laboratory Evaluation, Repeated Urine dipstick
Groupe Item: VITAL SIGNS