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  1. 1. Clinical Trial
  2. 2. Routine Documentation
  3. 3. Registry/Cohort Study
  4. 4. Quality Assurance
  5. 5. Data Standard
  6. 6. Patient-Reported Outcome
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234 Search results.

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Screening - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 9 itemgroups, 132 items, 1 language
Itemgroups: Inclusion/Exclusion criteria,Demography,Duration of Asthma,Vital Signs,12-Lead Electrocardiogram,Pulmonary function,Hematology,Clinical Chemistry,Urinalysis
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Eligibility NCT00525512 Pulmonary Disease, Chronic Obstructive - Eligibility

- 9/20/21 - 1 form, 2 itemgroups, 23 items, 2 languages
Itemgroups: Inclusion Criteria,Exclusion Criteria
ODM derived from http://clinicaltrials.gov/show/NCT00525512

Eligibility Chronic Obstructive Pulmonary Disease NCT00981851

- 9/20/21 - 1 form, 2 itemgroups, 13 items, 1 language
Itemgroups: Inclusion Criteria,Exclusion Criteria
Interaction in Chronic Obstructive Pulmonary Disease Experiment; ODM derived from: https://clinicaltrials.gov/show/NCT00981851

Follow-up - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 5 itemgroups, 42 items, 1 language
Itemgroups: Vital Signs Follow-up,12-Lead Electrocardiogram Follow-up,Hematology Follow-up,Clinical chemistry Follow-up,Urinalysis Follow-up
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 4, Day 1-2) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 16 itemgroups, 123 items, 1 language
Itemgroups: Investigational Product Day 1,Investigational Product Day 2,Hematology Day 1 Pre-Dose,Clinical chemistry Day 1 Pre-Dose,Urinalysis Day 1 Pre-Dose,Vital Signs Day 1,Vital Signs Day 2,12-Lead Electrocardiogram Day 1,12-Lead Electrocardiogram Day 2,FEV1 Day 1,Pharmacokinetic sampling Day 1,Potassium and Glucose Day 1,Pharmacokinetic Urine lnterval Collection Data Day 1,Hematology Day 1 Post-Dose,Clinical chemistry Day 1 Post-Dose,Urinalysis Day 1 Post-Dose
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 4, Day 7) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 13 itemgroups, 100 items, 1 language
Itemgroups: Hematology Day 7 Pre-Dose,Clinical chemistry Day 7 Pre-Dose,Urinalysis Day 7 Pre-Dose,Investigational Product Day 7,Vital Signs Day 7,12-Lead Electrocardiogram Day 7,FEV1 Day 7,Pharmacokinetic sampling Day 7,Potassium and Glucose Day 7,Pharmacokinetic Urine lnterval Collection Data Day 7,Hematology Day 7 Post-Dose,Clinical chemistry Day 7 Post-Dose,Urinalysis Day 7 Post-Dose
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 3, Day 7) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 13 itemgroups, 100 items, 1 language
Itemgroups: Hematology Day 7 Pre-Dose,Clinical chemistry Day 7 Pre-Dose,Urinalysis Day 7 Pre-Dose,Investigational Product Day 7,Vital Signs Day 7,12-Lead Electrocardiogram Day 7,FEV1 Day 7,Pharmacokinetic sampling Day 7,Potassium and Glucose Day 7,Pharmacokinetic Urine lnterval Collection Data Day 7,Hematology Day 7 Post-Dose,Clinical chemistry Day 7 Post-Dose,Urinalysis Day 7 Post-Dose
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 4, Day 3-6) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 6 itemgroups, 46 items, 1 language
Itemgroups: Vital Signs Day 3-6,12-Lead Electrocardiogram Day 3-6,FEV1 Day 3-6,Pharmacokinetic sampling Day 5-6,Potassium Day 5-6,Investigational Product Day 3-6
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 3, Day 3-6) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 6 itemgroups, 46 items, 1 language
Itemgroups: Vital Signs Day 3-6,12-Lead Electrocardiogram Day 3-6,FEV1 Day 3-6,Pharmacokinetic sampling Day 5-6,Potassium Day 5-6,Investigational Product Day 3-6
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 1, Day 1-2) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 16 itemgroups, 123 items, 1 language
Itemgroups: Investigational Product Day 1,Investigational Product Day 2,Hematology Day 1 Pre-Dose,Clinical chemistry Day 1 Pre-Dose,Urinalysis Day 1 Pre-Dose,Vital Signs Day 1,Vital Signs Day 2,12-Lead Electrocardiogram Day 1,12-Lead Electrocardiogram Day 2,FEV1 Day 1,Pharmacokinetic sampling Day 1,Potassium and Glucose Day 1,Pharmacokinetic Urine lnterval Collection Data Day 1,Hematology Day 1 Post-Dose,Clinical chemistry Day 1 Post-Dose,Urinalysis Day 1 Post-Dose
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 3, Day 1-2) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 16 itemgroups, 123 items, 1 language
Itemgroups: Investigational Product Day 1,Investigational Product Day 2,Hematology Day 1 Pre-Dose,Clinical chemistry Day 1 Pre-Dose,Urinalysis Day 1 Pre-Dose,Vital Signs Day 1,Vital Signs Day 2,12-Lead Electrocardiogram Day 1,12-Lead Electrocardiogram Day 2,FEV1 Day 1,Pharmacokinetic sampling Day 1,Potassium and Glucose Day 1,Pharmacokinetic Urine lnterval Collection Data Day 1,Hematology Day 1 Post-Dose,Clinical chemistry Day 1 Post-Dose,Urinalysis Day 1 Post-Dose
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

Main CRF (Treatment Period 2, Day 7) - GSK Milveterol COPD 100527

- 9/20/21 - 1 form, 13 itemgroups, 100 items, 1 language
Itemgroups: Hematology Day 7 Pre-Dose,Clinical chemistry Day 7 Pre-Dose,Urinalysis Day 7 Pre-Dose,Investigational Product Day 7,Vital Signs Day 7,12-Lead Electrocardiogram Day 7,FEV1 Day 7,Pharmacokinetic sampling Day 7,Potassium and Glucose Day 7,Pharmacokinetic Urine lnterval Collection Data Day 7,Hematology Day 7 Post-Dose,Clinical chemistry Day 7 Post-Dose,Urinalysis Day 7 Post-Dose
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

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