Clinical Trials

NCT01495026 | COMPLETED | PHASE1

63 participants

A Study Assessing a Range of Formulations of the Fixed Dose Combination Product Containing Dutasteride (0.5mg) and Tamsulosin Hydrochloride (0.2mg) to Find a Formulation Which is Bioequivalent to Harnal-D Tablets (Tamsulosin Hydrochloride, 0.2mg) in Healthy Male Subjects From North East Asia

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-11-06

Completion:

2012-04-03

Conditions

• Prostatic Hyperplasia

Interventions

• DRUG

No Results Yet

NCT01484054 | COMPLETED | NA

103 participants

Dispensing Evaluation of Subjective Comfort, Vision, and Handling of a New Lens Compared to a Marketed Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-11-30

Completion:

2012-02-29

Conditions

• Refractive Ametropia

Interventions

• DEVICE

Results Available

NCT01484028 | COMPLETED | NA

275 participants

Evaluation of the Performance of Two Contact Lenses Compared to a Marketed Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-11-30

Completion:

2012-02-29

Conditions

• Refractive Ametropia

Interventions

• DEVICE

Results Available

NCT01482819 | COMPLETED | NA

21 participants

Evaluation of Daytime Corneal Swelling During Wear of Galyfilcon A Lenses

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-10-01

Completion:

2011-12-01

Conditions

• Myopia

Interventions

• DEVICE
• OTHER

Results Available

NCT01480609 | COMPLETED | PHASE1

8 participants

Effect of Haemodialysis on the Pharmacokinetics of Ezogabine/Retigabine and Its N-acetyl Metabolite

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-11-30

Completion:

2012-04-24

Conditions

• Epilepsy

Interventions

• DRUG

No Results Yet

NCT01471678 | COMPLETED | PHASE1

27 participants

Bioavailability of Two Combination Products of Dutasteride (0.5mg) and Tamsulosin Hydrochloride (0.2mg) in Asian Males.

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-06-30

Completion:

2011-09-07

Conditions

• Prostatic Hyperplasia

Interventions

• DRUG

No Results Yet

NCT01467557 | COMPLETED

1171 participants

Daily Disposable Performance of 1•DAY ACUVUE® TruEye™ and 1•DAY ACUVUE® MOIST® With LACREON® TECHNOLOGY

Study Type:

OBSERVATIONAL

Last Updated:

2018-06-19

Start Date:

2011-10-31

Completion:

2013-10-31

Conditions

• Myopia
• Hyperopia

Interventions

• DEVICE

Results Available

NCT01462669 | COMPLETED | PHASE1

1 participants

Crossover Study to Evaluate the Pharmacokinetics of Ezogabine/Retigabine in Taiwanese Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2012-04-10

Completion:

2012-06-27

Conditions

• Epilepsy

Interventions

• DRUG

No Results Yet

NCT01462604 | COMPLETED

27 participants

Pilot Study of Patient's Adherence to TYKERB™/TYVERB™ + Capecitabine in Metastatic Breast Cancer

Study Type:

OBSERVATIONAL

Last Updated:

2018-06-19

Start Date:

2011-11-23

Completion:

2013-01-01

Conditions

• Cancer

Interventions

• OTHER

No Results Yet

NCT01444313 | COMPLETED | NA

40 participants

Prospective Study of the Health Benefits of Ultra-Violet Filtering Contact Lenses

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-01-31

Completion:

2013-03-31

Conditions

• Refractive Errors

Interventions

• DEVICE

No Results Yet

NCT01444287 | COMPLETED | NA

22 participants

Daytime Corneal Swelling During Wear of Narafilcon B Lenses

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-01-31

Completion:

2010-02-28

Conditions

• Myopia

Interventions

• DEVICE
• OTHER

Results Available

NCT01437319 | COMPLETED | PHASE1/PHASE2

289 participants

Mucin Balls and Corneal Inflammation Events

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-09-30

Completion:

2014-02-28

Conditions

• Corneal Inflammation
• Corneal Infiltrative Events

Interventions

• DEVICE
• OTHER

Results Available

NCT01435915 | COMPLETED | PHASE1

24 participants

Ropinirole PR Pharmacokinetics Study Among Chinese Healthy Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-06-28

Completion:

2010-08-05

Conditions

• Parkinson Disease

Interventions

• DRUG

No Results Yet

NCT01406873 | COMPLETED | PHASE2

42 participants

Clinical Efficacy Trial of Mexiletine for Myotonic Dystrophy Type 1

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-06-30

Completion:

2017-02-28

Conditions

• Myotonic Dystrophy

Interventions

• DRUG

Results Available

NCT01371682 | COMPLETED | PHASE1

50 participants

A Study Conducted in Healthy Subjects to Demonstrate Bioequivalence Between Ropinirole Prolonged Release Tablets Manufactured at Crawley and Aranda

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2009-09-18

Completion:

2009-12-02

Conditions

• Parkinson Disease

Interventions

• DRUG

No Results Yet

NCT01364805 | COMPLETED | PHASE1

14 participants

New Treatment Option for Pancreatic Cancer

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-04-30

Completion:

2015-10-31

Conditions

• Pancreatic Cancer

Interventions

• DRUG

No Results Yet

NCT01332513 | COMPLETED | PHASE1

36 participants

An Open Label, Randomised, Repeat Dose Study to Assess the Pharmacokinetic Performance of Five Ezogabine/Retigabine Modified Release (MR) Formulations at Steady State Compared to the Immediate Release (IR) Formulation.

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-02-10

Completion:

2011-05-23

Conditions

• Epilepsy

Interventions

• DRUG

No Results Yet

NCT01290237 | TERMINATED | NA

59 participants

Use of a Loading Dose of Vancomycin in Pediatric Dosing

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2011-02-28

Completion:

2012-02-29

Conditions

• Infection

Interventions

• DRUG

Results Available

NCT01281930 | COMPLETED | NA

156 participants

Abscess Packing Versus Wick Placement After Incision and Drainage

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2009-06-30

Completion:

2015-11-30

Conditions

• Superficial Abscess Packing

Interventions

• PROCEDURE

No Results Yet

NCT01248897 | COMPLETED

158 participants

Study of Biomarker Profiles in Asia Pacific erb2+/HER2 Breast Cancer Patients Treated With Lapatinib

Study Type:

OBSERVATIONAL

Last Updated:

2018-06-19

Start Date:

2010-08-17

Completion:

2013-12-01

Conditions

• Neoplasms, Metastasis

Interventions

• OTHER

No Results Yet

NCT01244893 | COMPLETED | NA

44 participants

Study of ACUVUE® ADVANCE® PLUS Contact Lenses.

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-10-31

Completion:

2010-11-30

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01244529 | COMPLETED | NA

41 participants

Comparison of Lens Fit and Lens Power of a New Contact Lens to Two Marketed Contact Lenses in a Population of Soft Contact Lens Wearers

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-09-01

Completion:

2010-11-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01244516 | COMPLETED | NA

540 participants

Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-09-01

Completion:

2010-11-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01228591 | COMPLETED | NA

38 participants

Pilot Dispensing Evaluation of a Plus Power Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-10-31

Completion:

2010-11-30

Conditions

• Hyperopia

Interventions

• DEVICE

Results Available

NCT01224639 | COMPLETED | PHASE1

96 participants

Safety and Immunogenicity Study to Assess TDV, a Live Attenuated Tetravalent Vaccine for Prevention of Dengue Fever

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-10-11

Completion:

2011-06-09

Conditions

• Dengue Fever

Interventions

• BIOLOGICAL

Results Available

NCT01205243 | COMPLETED

671 participants

ZIAGEN® Post-marketing Surveillance

Study Type:

OBSERVATIONAL

Last Updated:

2018-06-19

Start Date:

2010-11-01

Completion:

2015-02-01

Conditions

• Infection, Human Immunodeficiency Virus I

Interventions

• DRUG

No Results Yet

NCT01192542 | COMPLETED | NA

39 participants

Pilot Evaluation of a New Galyfilcon A Lens Prototype and Enfilcon A Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-08-31

Completion:

2010-09-30

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01180998 | COMPLETED | NA

200 participants

Clinical Evaluation of Two Toric Contact Lenses in Current Non-toric Lens Users

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-06-01

Completion:

2010-10-01

Conditions

• Astigmatism

Interventions

• DEVICE

Results Available

NCT01180985 | COMPLETED | NA

53 participants

Dispensing Evaluation of a Galyfilcon A Prototype Lens and a Marketed Contact Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-06-01

Completion:

2010-07-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01180777 | COMPLETED | NA

95 participants

Dispensing Evaluation of Printed Etafilcon A With Polyvinylpyrrolidone (PVP)

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-07-01

Completion:

2010-08-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01163760 | COMPLETED | NA

50 participants

Clinical Evaluation of Two Daily Disposable Contact Lenses

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2007-09-30

Completion:

2007-09-30

Conditions

• Refractive Error

Interventions

• DEVICE

Results Available

NCT01155323 | COMPLETED | NA

118 participants

Two Week Cross-Over Study Comparing Two Daily Disposable Contact Lenses

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-03-01

Completion:

2010-06-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01151371 | COMPLETED | NA

452 participants

Clinical Evaluation Of Two Daily Disposable Contact Lenses And A Monthly Replacement Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-02-01

Completion:

2010-04-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01120782 | COMPLETED | NA

45 participants

Non-dispensing Study to Check Prescription Equivalence of Two Daily Disposable Toric Contact Lens Types

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-02-01

Completion:

2010-02-01

Conditions

• Astigmatism

Interventions

• DEVICE

Results Available

NCT01094743 | COMPLETED | NA

52 participants

Dispensing Evaluation of a Prototype Contact Lens and a Marketed Contact Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-02-01

Completion:

2010-03-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01094730 | COMPLETED | NA

185 participants

Pilot Evaluation of a New Galyfilcon A Contact Lens Compared to a Marketed Galyfilcon A Contact Lens

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-02-01

Completion:

2010-04-01

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01093625 | COMPLETED | NA

157 participants

Assessment of Daily Disposable Silicone Hydrogel Lens Wear

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-01-31

Completion:

2011-04-30

Conditions

• Myopia

Interventions

• DEVICE

Results Available

NCT01055613 | COMPLETED | NA

312 participants

Investigational Multi-purpose Contact Lens Care Solution.

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2009-11-30

Completion:

2010-05-31

Conditions

• Contact Lens Wear

Interventions

• DEVICE

Results Available

NCT01055457 | COMPLETED | NA

315 participants

Vistakon Investigational Multi-purpose Contact Lens Care Solution.

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2009-11-01

Completion:

2010-05-01

Conditions

• Contact Lens Wear

Interventions

• DEVICE

Results Available

NCT01055132 | COMPLETED | NA

70 participants

Dispensing Evaluation of New Daily Disposable Toric Soft Contact Lens.

Study Type:

INTERVENTIONAL

Last Updated:

2018-06-19

Start Date:

2010-01-31

Completion:

2010-02-28

Conditions

• Astigmatism

Interventions

• DEVICE

Results Available