Clinical Trials

NCT00454896 | COMPLETED | PHASE3

739 participants

A Multicenter VESIcare® Efficacy and Safety Study for the Treatment of Urgency Associated With Overactive Bladder (OAB)

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2004-05-31

Completion:

2005-09-30

Conditions

• Urinary Bladder, Overactive

Interventions

• DRUG

No Results Yet

NCT00454740 | COMPLETED | PHASE3

441 participants

Efficacy & Safety Study of VESIcare® (Solifenacin Succinate) in Patients Wishing to Switch From Detrol LA® for Treatment of Overactive Bladder

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2004-06-30

Completion:

2005-08-31

Conditions

• Urinary Bladder, Overactive

Interventions

• DRUG

No Results Yet

NCT00431158 | COMPLETED | NA

224 participants

ARDSnet Protocol vs. Open Lung Approach in ARDS

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2007-01-31

Completion:

2012-09-30

Conditions

• Respiratory Distress Syndrome, Adult

Interventions

• OTHER

No Results Yet

NCT00397605 | WITHDRAWN | NA

0 participants

Cannabinoids in Bipolar Affective Disorder

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2006-11-30

Completion:

2013-12-31

Conditions

• Bipolar Affective Disorder

Interventions

• DRUG

No Results Yet

NCT00337558 | COMPLETED | PHASE4

643 participants

A Study of Solifenacin With Bladder Training Versus Solifenacin Alone in Patients With Overactive Bladder (SOLAR)

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2006-05-31

Completion:

2007-05-31

Conditions

• Overactive Bladder
• Urinary Incontinence
• Urge Incontinence

Interventions

• DRUG
• BEHAVIORAL

No Results Yet

NCT00333112 | COMPLETED | PHASE4

398 participants

A Study to Evaluate Solifenacin Succinate in Combination With Tamsulosin for the Treatment of Residual Overactive Bladder Symptoms (OAB) in Men.

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2006-05-31

Completion:

2007-01-31

Conditions

• Urinary Incontinence

Interventions

• DRUG

No Results Yet

NCT00315939 | COMPLETED | NA

120 participants

Improving Control and Reducing the Risk of Hypoglycemic Episodes in Type 1 Diabetes

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2006-01-31

Completion:

2009-12-31

Conditions

• Diabetes Mellitus, Type 1

Interventions

• DEVICE

Results Available

NCT00290290 | COMPLETED | PHASE3

849 participants

Efficacy Study of Antiseptic Preoperative Scrubs in Prevention of Postoperative Infections

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2003-09-30

Completion:

2008-05-31

Conditions

• Postoperative Wound Infection

Interventions

• DRUG

Results Available

NCT00106496 | COMPLETED | PHASE4

410 participants

A Multi-Center Study of Short and Long-term Use of Protopic Ointment in Patients With Atopic Dermatitis

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2004-10-31

Completion:

2006-07-31

Conditions

• Dermatitis, Atopic

Interventions

• DRUG

No Results Yet

NCT00106288 | COMPLETED | PHASE3

637 participants

Micafungin Versus AmBisome in Invasive Candidiasis and Candidemia

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2003-01-31

Completion:

2005-12-31

Conditions

• Candidiasis

Interventions

• DRUG

No Results Yet

NCT00105144 | COMPLETED | PHASE3

611 participants

Study of Micafungin in Patients With Invasive Candidiasis or Candidemia

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2004-09-30

Completion:

2006-04-30

Conditions

• Candidiasis
• Candidemia

Interventions

• DRUG

No Results Yet

NCT00074737 | COMPLETED | PHASE2

53 participants

Dosing Study of Ara-C/EL625/Idarubicin in Refractory and Relapsed AML

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-18

Start Date:

2004-04-30

Completion:

2007-05-31

Conditions

• Acute Myelogenous Leukemia

Interventions

• DRUG

No Results Yet

NCT02243410 | COMPLETED

62 participants

Visual Analogue Scale - a Quality Assurance Study

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2014-03-31

Completion:

2014-09-30

Conditions

• Surgery

No Results Yet

NCT02243345 | COMPLETED

204 participants

Delayed Recompression for Decompression Sickness

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2013-09-30

Completion:

2014-06-30

Conditions

• Recompression Treatment After Decompression Sickness

No Results Yet

NCT02243241 | COMPLETED | PHASE1

208 participants

The Effect of Hydrocodone Bitartrate (HYD) Extended-Release Tablets on QT /QTc Intervals in Healthy Adult Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2012-11-30

Completion:

2013-05-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02243228 | UNKNOWN | PHASE2

42 participants

Inhalation of Granulocyte-macrophage Colony-stimulating Factor (GM-CSF) for Autoimmune Pulmonary Alveolar Proteinosis (PAP)

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2014-08-31

Completion:

2017-08-31

Conditions

• Autoimmune Pulmonary Alveolar Proteinosis

Interventions

• DRUG

No Results Yet

NCT02243163 | UNKNOWN | NA

40 participants

Effect of Yoga on Life Quality and Immunity in Breast Cancer Patients After Operation and or Chemotherapy

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2014-05-31

Completion:

2015-04-30

Conditions

• Female Breast Carcinoma

Interventions

• BEHAVIORAL

No Results Yet

NCT02243137 | COMPLETED | PHASE1

30 participants

Study of Platelet Function After Administration of Aspirin Versus Lysine Acetylsalicylate

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2013-05-31

Completion:

2014-06-30

Conditions

• Adverse Effect of Antithrombotic Drugs

Interventions

• DRUG

No Results Yet

NCT02243085 | UNKNOWN

126 participants

Predictors of de Novo Urge Urinary Incontinence After Photoselective Vaporization of the Prostate

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2014-08-31

Completion:

2014-10-31

Conditions

• Prostatic Hyperplasia
• Urgency
• Urinary Incontinence

No Results Yet

NCT02242877 | COMPLETED

3320 participants

TELSYS - TELmisartan Effectiveness in Isolated SYStolic Hypertension Versus Systolic/Diastolic Hypertension Patients Aged 55 or Older

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2006-02-28

Completion:

2006-10-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242864 | COMPLETED

1527 participants

Study to Evaluate the Effect of the Treatment With Micardis® or MicardisPlus® on Blood Pressure

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2006-01-31

Completion:

2006-10-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242851 | COMPLETED

5018 participants

Study Describing the Hypertensive Population Treated With Telmisartan and Conditions of Use by Medical Practitioners and Patients

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2004-09-30

Completion:

2005-05-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242838 | COMPLETED

6336 participants

Post-Marketing Surveillance of Micardis® (Telmisartan) in Patients With Hypertension

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2003-09-30

Completion:

2006-09-30

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242825 | COMPLETED

8148 participants

Study to Evaluate the Effect of Micardis® / MicardisPlus® on Metabolic Parameters in Patients With Essential Hypertension and Diabetes Mellitus

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2006-01-31

Completion:

2006-10-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242812 | TERMINATED | PHASE4

24 participants

Telmisartan Effectiveness on Left Ventricular Mass Reduction (TELMAR) as Assessed by MRI, in Patients With Mild to Moderate Hypertension

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2003-09-30

Completion:

2004-10-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242747 | COMPLETED | NA

100 participants

Safety and Tolerability Study of Ingenol Mebutate Compared to 5-FU to Treat Facial Actinic Keratosis

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2014-05-31

Completion:

2014-07-31

Conditions

• Actinic Keratosis

Interventions

• DRUG

No Results Yet

NCT02242708 | UNKNOWN | NA

40 participants

The Effectiveness of Autonomic Nervous System, Sleep Quality, and Immune Regulation for Shift Nurses Practicing Alternative Nostril Breathing

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2013-10-31

Completion:

2014-12-31

Conditions

• Shift Nurses

Interventions

• BEHAVIORAL

No Results Yet

NCT02242552 | UNKNOWN

30 participants

Personalized Targeted Therapy in Refractory or Relapsed Cancer in Childhood

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2014-06-30

Completion:

2016-06-30

Conditions

• Pediatric Cancer

No Results Yet

NCT02242461 | COMPLETED | PHASE2

57 participants

Rhodiola Crenulata as an Adjunctive Therapy in COPD

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2012-05-31

Completion:

2013-07-31

Conditions

• COPD

Interventions

• DRUG

No Results Yet

NCT02242422 | UNKNOWN

200 participants

Serial Changes in Micturition Symptoms, Urine Flow and Bladder Voiding Efficiency Following Transobturator Tape Surgery

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2014-08-31

Completion:

2014-11-30

Conditions

• Stress Urinary Incontinence

No Results Yet

NCT02242396 | COMPLETED

5248 participants

A Study of a Hypertensive Population Under Treatment With Micardis® and Micardis Plus® to Control the Early Morning BP Rise (SURGE II)

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2005-08-31

Completion:

2007-11-30

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242383 | COMPLETED

13248 participants

Evaluation of Efficacy and Tolerability of Micardis® / MicardisPlus® Under Usual Daily-practice Prescribing in Patients With Hypertension

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2005-01-31

Completion:

2005-10-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242370 | COMPLETED | PHASE4

3045 participants

Effectiveness of MICARDIS® (Telmisartan) on Blood Pressure Control and Quality of Live in Patients With Essential Hypertension

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

1999-09-30

Completion:

2000-11-30

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242357 | COMPLETED

14553 participants

Study to Evaluate Efficacy and Tolerability of Micardis®/Micardis® Plus in Patients With Hypertension

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2003-01-31

Completion:

2003-07-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242331 | COMPLETED

19805 participants

Post-marketing Study to Supplement Data on Safety, Tolerability and Efficacy of Micardis® With Special Emphasis on the Control of Blood Pressure

Study Type:

OBSERVATIONAL

Last Updated:

2014-09-17

Start Date:

2001-06-30

Completion:

2002-05-31

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242318 | COMPLETED | PHASE4

440 participants

Study to Evaluate Efficacy of Micardis® (Telmisartan) and Valsartan in Patients With Mild-to-moderate Hypertension After Missing One Dose Using Ambulatory Blood Pressure Monitoring

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2001-09-30

Completion:

2002-09-30

Conditions

• Hypertension

Interventions

• DRUG

No Results Yet

NCT02242279 | COMPLETED | PHASE2

37 participants

Study to Evaluate Efficacy and Safety of Inhaled BEA 2180 BR in COPD Patients

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2004-06-30

Completion:

2004-12-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02242253 | COMPLETED | PHASE2

97 participants

Free Combinations of Tiotropium Inhalation Powder Capsule + Salmeterol Metered Dose Inhaler, Tiotropium Inhalation Powder Capsule and Salmeterol Metered Dose Inhaler in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2003-09-30

Completion:

2004-07-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02242240 | COMPLETED | PHASE2

95 participants

Lung Function Changes Following the Addition of Formoterol to Tiotropium in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2001-03-31

Completion:

2001-12-31

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02242227 | COMPLETED | PHASE2

111 participants

Efficacy, Pharmacokinetics and Safety Comparison of Salmeterol Inhalation Powder Administered Via the HandiHaler® 2 and Serevent® Diskus® in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-09-17

Start Date:

2005-09-30

Completion:

2006-02-28

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet