Clinical Trials

NCT02172573 | COMPLETED | PHASE3

315 participants

Safety and Efficacy of Pramipexole and Bromocriptine Combined With L-dopa in Parkinson's Disease

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

1999-04-30

Completion:

2000-07-31

Conditions

• Parkinson Disease

Interventions

• DRUG

No Results Yet

NCT02172547 | COMPLETED

10821 participants

Effect of Spiriva® on Health-related Quality of Life in Chronic Obstructive Pulmonary Disease (COPD) Patients Who Stopped Smoking During Treatment.

Study Type:

OBSERVATIONAL

Last Updated:

2014-06-24

Start Date:

2006-04-30

Completion:

2007-01-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172534 | COMPLETED | PHASE1

113 participants

Safety, Tolerability and Pharmacokinetics of Tiotropium in Cystic Fibrosis Patients

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2006-09-30

Completion:

2008-09-30

Conditions

• Cystic Fibrosis

Interventions

• DRUG

No Results Yet

NCT02172521 | COMPLETED

1536 participants

Effect of Spiriva® 18 Microgram on Health-related Quality of Life and Physical Functioning in Patients With Chronic Obstructive Pulmonary Disease (COPD) and Proven Hyperinflation

Study Type:

OBSERVATIONAL

Last Updated:

2014-06-24

Start Date:

2006-01-31

Completion:

2006-10-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172508 | TERMINATED | PHASE4

15 participants

Effect of Tiotropium Inhalation Capsules on Exercise Tolerance, Daily Activity and Dyspnoea in Patients With Chronic Obstructive Pulmonary Disease (COPD) Participating in 3 Weeks of Pulmonary Rehabilitation

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2004-01-31

Completion:

2004-03-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172482 | COMPLETED

63127 participants

Spiriva® in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

OBSERVATIONAL

Last Updated:

2014-06-24

Start Date:

2002-06-30

Completion:

2003-10-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172469 | COMPLETED | PHASE3

215 participants

Efficacy and Safety of Tiotropium and Atrovent in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2001-05-31

Completion:

2002-04-30

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172456 | COMPLETED | PHASE3

22 participants

Evaluation of the Lung Deposition Rate and Distribution Pattern of Tiotropium Via HandiHalerTM in Healthy Subjects and Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2002-05-31

Completion:

2002-10-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172417 | COMPLETED | PHASE1

18 participants

Tiotropium in Combination With Concomitant Cimetidine or Ranitidine in Healthy Male and Female Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2000-07-31

Completion:

2000-11-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172378 | COMPLETED | PHASE3

116 participants

12-week Treatment With Inhaled Tiotropium (18 mcg Once Daily) on Lung Function and Static Lung Volumes in Stable, Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD) Patients. Correlation to Dyspnoea Scales

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2000-05-31

Completion:

2002-01-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172352 | COMPLETED | PHASE2

28 participants

Dose Ranging Study of Ba 679 BR Inhalation Powder in Chronic Obstructive Pulmonary Disease (COPD) Patients

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

1998-07-31

Completion:

1999-05-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172339 | COMPLETED | PHASE1

24 participants

The Pharmacokinetic, Safety and Tolerability of Tiotropium in Outpatients With Renal Impairment in Comparison to Healthy Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

1998-04-30

Completion:

1998-12-31

Conditions

• Renal Insufficiency

Interventions

• DRUG

No Results Yet

NCT02172326 | COMPLETED | PHASE3

29 participants

Pharmacokinetic Study in Elderly Patients With Chronic Obstructive Bronchitis (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

1998-02-28

Completion:

1998-09-30

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172300 | COMPLETED | PHASE3

198 participants

Effect of Tiotropium on Exercise Tolerance in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

1999-06-30

Completion:

2000-11-30

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172287 | COMPLETED | PHASE3

623 participants

Multiple Dose Comparison of Tiotropium Inhalation Capsules, Salmeterol Inhalation Aerosol and Placebo in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

1999-02-28

Completion:

2000-05-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02172274 | COMPLETED | PHASE1

8 participants

BI 10773 Administered as Oral Solution to Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2008-06-30

Completion:

2008-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172261 | COMPLETED | PHASE1

16 participants

Relative Bioavailability of BI 10773 and Glimepiride in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-04-30

Completion:

2009-06-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172248 | COMPLETED | PHASE1

16 participants

Relative Bioavailability BI 10773 and Metformin in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-01-31

Completion:

2009-03-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172235 | COMPLETED | PHASE1

20 participants

Relative Bioavailability of Pioglitazone After Co-administration With Different Doses of BI 10773 in Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2010-04-30

Completion:

2010-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172222 | COMPLETED | PHASE1

16 participants

Relative Bioavailability of BI 10773 and Linagliptin in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-07-31

Completion:

2009-09-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172209 | COMPLETED | PHASE1

14 participants

Bioavailability and Pharmacokinetics of BI 10773 Tablet in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2008-01-31

Completion:

2008-02-29

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172196 | COMPLETED | PHASE1

16 participants

Bioavailability of BI 10773 and Sitagliptin in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-05-31

Completion:

2009-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172183 | COMPLETED | NA

119 participants

CBT Group for Adolescents With ADHD: a Randomized Controlled Trial

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2012-04-30

Completion:

2014-03-31

Conditions

• Attention Deficit Hyperactivity Disorder

Interventions

• DRUG
• BEHAVIORAL

No Results Yet

NCT02172170 | COMPLETED | PHASE1

72 participants

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Oral Doses of BI 10773 in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2007-01-31

Completion:

2007-03-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172157 | COMPLETED | PHASE1

11 participants

Investigation of the Metabolism and Pharmacokinetics of [14C]BI 1744 CL and [14C]BI 1744 CL Administered as an Oral Solution in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2008-02-29

Completion:

2008-04-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172144 | COMPLETED | PHASE1

24 participants

Via Respimat® Inhaled BI 1744 CL Compared to Moxifloxacin and Placebo in Healthy Male and Female Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2007-06-30

Completion:

2007-10-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172131 | TERMINATED | PHASE1

64 participants

Safety, Tolerability and Pharmacokinetics Study of BI 1744 CL in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2006-10-31

Completion:

2007-02-28

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172118 | COMPLETED | PHASE1

22 participants

BI 1744 CL in Patients With Severe Renal Impairment in Comparison to Subjects With Normal Renal Function

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-08-31

Completion:

2009-12-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172105 | COMPLETED | PHASE1

36 participants

Multiple Rising Inhalative Doses of BI 1744 CL in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2008-01-31

Completion:

2008-05-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02172079 | COMPLETED | NA

42 participants

Mobilization With Movement for Shoulder Impingement

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2013-01-31

Completion:

2014-01-31

Conditions

• Shoulder Impingement Syndrome

Interventions

• OTHER

No Results Yet

NCT02171975 | COMPLETED | NA

100 participants

Ultrasound - Guided Paramedian Techniques in Spinal Anesthesia

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2014-02-28

Completion:

2014-05-31

Conditions

• Anaesthesia

Interventions

• PROCEDURE

No Results Yet

NCT02171936 | UNKNOWN

800 participants

Chronic Pain and Social Vulnerability: Prevalence and Predictive Factors of the Social Vulnerability in Evaluation and Treatment of the Pain Center (CETD)

Study Type:

OBSERVATIONAL

Last Updated:

2014-06-24

Start Date:

2014-05-31

Completion:

2016-04-30

Conditions

• Chronic Pain

Interventions

• OTHER

No Results Yet

NCT02171871 | COMPLETED | PHASE1

20 participants

Effects Of Passive Smoking On The Respiratory System Mechanics Of Healthy Non-Smokers In Different Body Positions

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2010-01-31

Completion:

2013-12-31

Conditions

• PASSIVE SMOKING ,
• RESPIRATORY SYSTEM MECHANICS,

Interventions

• OTHER

No Results Yet

NCT02171858 | UNKNOWN

28 participants

Multivariate Analysis of Serum High Sensitivity C-Reactive Protein in Patients With Acute Phase Stroke

Study Type:

OBSERVATIONAL

Last Updated:

2014-06-24

Start Date:

2013-06-30

Completion:

2015-01-31

Conditions

• Stroke
• National Institutes of Health Stroke Scale
• Serum High Sensitivity C-Reactive Protein

No Results Yet

NCT02171832 | COMPLETED | PHASE1

32 participants

Single Dose of BI 1744 CL in Patients With Mild and Moderate Hepatic Impairment Compared to Subjects With Normal Hepatic Function

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-07-31

Completion:

2009-12-31

Conditions

• Healthy
• Liver Diseases

Interventions

• DRUG

No Results Yet

NCT02171806 | COMPLETED | PHASE1

47 participants

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of BI 1744 CL in Healthy Male and Female Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2006-01-31

Completion:

2006-09-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02171793 | COMPLETED | PHASE1

24 participants

Single Rising Peroral Doses of BI 1744 CL in Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2007-06-30

Completion:

2007-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02171780 | COMPLETED | PHASE1

122 participants

A Study to Assess Safety, Tolerability and Pharmacokinetics of Single Rising Inhaled Doses of BI 1744 CL in Healthy Male and Female Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2005-02-28

Completion:

2005-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02171767 | COMPLETED | PHASE1

48 participants

Safety and Tolerability of 4 Different Dosage Strengths of BIBW 2992 Tablets to Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-08-31

Completion:

2009-10-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02171754 | COMPLETED | PHASE1

22 participants

Relative Bioavailability of a Single-dose Administration of BIBW 2992 and Multiple-dose Administration of Ritonavir in Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-06-24

Start Date:

2009-09-30

Completion:

2009-12-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet