Clinical Trials

NCT02194764 | COMPLETED | NA

8 participants

An Adherence Tool to Manage Narcotic -Addicted HIV Patients

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2014-06-30

Completion:

2014-07-31

Conditions

• Healthy Adults

Interventions

• DRUG

No Results Yet

NCT02194673 | COMPLETED | NA

20 participants

Acute Effects of Natural and Interesterified Fats-margarine on Lipemic and Insulinemic Response

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2012-01-31

Completion:

2012-12-31

Conditions

• Healthy

Interventions

• OTHER

No Results Yet

NCT02194556 | UNKNOWN | PHASE4

100 participants

Sequential and Maintenance Icotinib Plus Chemotherapy Versus Icotinib Maintenance After Chemotherapy in Advanced NSCLC

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2014-07-31

Completion:

2017-07-31

Conditions

• EGFR Positive Non-small Cell Lung Cancer
• Adenocarcinoma

Interventions

• DRUG

No Results Yet

NCT02194543 | COMPLETED

20 participants

High-Definition 3D Visualization System for Ophthalmic Surgery

Study Type:

OBSERVATIONAL

Last Updated:

2014-07-18

Start Date:

2014-03-31

Completion:

2014-07-31

Conditions

• Cataract

No Results Yet

NCT02194361 | COMPLETED | PHASE2

119 participants

Efficacy of a Standardised Bilberry Extract in Improving the Night Vision of Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

1999-12-31

Completion:

2000-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02194309 | COMPLETED | PHASE1

24 participants

Safety, Tolerability and Pharmacokinetics of Single and Multiple Oral Doses of 40 mg Telmisartan/5 mg Amlodipine and 80 mg Telmisartan/5 mg Amlodipine in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2006-09-30

Completion:

2006-12-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02194296 | COMPLETED | PHASE1

20 participants

Relative Bioavailability of Ambroxol Hydrochloride Lozenge in Comparison to Ambroxol Hydrochloride Syrup (Mucosolvan®) in Healthy Female and Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

1999-06-30

Completion:

1999-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02194270 | COMPLETED | PHASE1

24 participants

Relative Bioavailability of Ambroxol Hydrochloride of Soft Pastilles Compared to Ambroxol Hydrochloride Syrup in Healthy Male and Female Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2004-09-30

Completion:

2005-02-28

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02194257 | COMPLETED | PHASE1

12 participants

Investigation of the Metabolism and Pharmacokinetics of Ambroxol in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2008-10-31

Completion:

2008-12-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02194218 | COMPLETED | PHASE1

48 participants

Pharmacokinetic Properties of Nevirapine Extended Release Tablets When Administered Orally in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2009-09-30

Completion:

2009-11-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02194205 | TERMINATED | PHASE3

360 participants

Comparison of Safety and Efficacy of COMBIVENT HFA to COMBIVENT (CFC) in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2000-10-31

Completion:

2001-06-30

Conditions

• Pulmonary Disease, Chronic Obstructive

Interventions

• DRUG

No Results Yet

NCT02194179 | COMPLETED | PHASE1

92 participants

Bioavailability of 2 Different Nevirapine Extended Release Formulations Compared to Viramune® in HIV-1 Infected Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2006-12-31

Completion:

2007-05-31

Conditions

• HIV Infections

Interventions

• DRUG
• OTHER

No Results Yet

NCT02194153 | COMPLETED

351 participants

Surveillance of Patients With Suspected Acute Myocardial Infarction That Receive Early Inhospital Thrombolysis With Metalyse

Study Type:

OBSERVATIONAL

Last Updated:

2014-07-18

Start Date:

2001-05-31

Completion:

2003-03-31

Conditions

• Myocardial Infarction

Interventions

• DRUG

No Results Yet

NCT02194140 | UNKNOWN | NA

200 participants

Improvement of Appendix Identification and Appendicitis Diagnosis in us After Administration of Oral Contrast Medium

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2014-07-31

Completion:

2015-07-31

Conditions

• Appendicitis

Interventions

• OTHER

No Results Yet

NCT02194114 | COMPLETED | NA

13 participants

Dietary Protein Requirements in Hemodialysis Patients

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2004-01-31

Completion:

2008-01-31

Conditions

• Chronic Renal Failure
• End-Stage Renal Disease

Interventions

• OTHER

No Results Yet

NCT02194101 | UNKNOWN

30 participants

Supernormal Goal for Proximal Femur Fracture

Study Type:

OBSERVATIONAL

Last Updated:

2014-07-18

Start Date:

2014-08-31

Completion:

2015-04-30

Conditions

• Femoral Fractures

Interventions

• PROCEDURE

No Results Yet

NCT02194023 | COMPLETED | PHASE2

200 participants

Clinical Effects of Two New Chlorhexidine Digluconate Formulations: 0.12% and 0.03%.

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2011-09-30

Completion:

2013-07-31

Conditions

• Dental Plaque
• Side Effects

Interventions

• DRUG

No Results Yet

NCT02193919 | COMPLETED

30 participants

A Single-Center, Prospective, Pilot Study to Compare the Effect of Diet in Overweight or Obese Patients With Psoriasis on Light Therapy

Study Type:

OBSERVATIONAL

Last Updated:

2014-07-18

Start Date:

2007-03-31

Completion:

2008-05-31

Conditions

• Psoriasis

No Results Yet

NCT02193906 | UNKNOWN | NA

75 participants

Neuropsychological Profile of a Patient's Group With Multiple Sclerosis and Effect of a Cognitive Rehabilitation Program

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2012-12-31

Completion:

2013-06-30

Conditions

• Cognitive Dysfunction

Interventions

• OTHER

No Results Yet

NCT02193893 | UNKNOWN | PHASE1

50 participants

Biological Treatment of Amyotrophic Lateral Sclerosis

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2010-01-31

Completion:

2017-07-31

Conditions

• Amyotrophic Lateral Sclerosis

Interventions

• OTHER

No Results Yet

NCT02193854 | COMPLETED | NA

441 participants

Teledermatology Solution Through Mobile Phone in Rural Mongolia

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2013-09-30

Completion:

2014-01-31

Conditions

• Social Distance

Interventions

• DEVICE

No Results Yet

NCT02193672 | WITHDRAWN | PHASE1

0 participants

A Pilot, Exploratory, Non-Randomized Study of PET/CT With the Investigational Agent [18F] Fluciclatide to Correlate With Response to Anti-Cancer Therapy

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2014-08-31

Completion:

2020-08-31

Conditions

• Advanced Cancers

Interventions

• DRUG
• PROCEDURE
• BEHAVIORAL

No Results Yet

NCT02193308 | COMPLETED | PHASE1

84 participants

Bioequivalence of Telmisartan/Amlodipine Fixed Dose Combination Compared With Its Monocomponents in Healthy Male and Female Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2007-09-30

Completion:

2007-11-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182453 | COMPLETED | PHASE1

48 participants

Single Rising Oral Doses of BI 10773 in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2008-06-30

Completion:

2008-08-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182414 | COMPLETED | PHASE1

42 participants

Relative Bioavailability of BI 207127 Trial Formulation II Prototypes Versus BI 207127 Trial Formulation I in Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2009-05-31

Completion:

2009-09-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182401 | TERMINATED | PHASE1

37 participants

Multiple Doses of BI 207127 NA, BI 201335 NA Followed by the Combination of BI 207127 NA and BI 201335 NA in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2009-07-31

Completion:

2009-08-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182388 | COMPLETED | PHASE1

82 participants

Single Rising Oral Doses of BI 207127 NA as Powder in the Bottle in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2007-01-31

Completion:

2007-05-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182375 | COMPLETED | PHASE1

24 participants

Effect of BI 201335 Mediated UGT1A1 (Uridine-diphosphate-glucuronosyltransferases) Inhibition in Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2010-01-31

Completion:

2010-03-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182362 | COMPLETED | PHASE1

39 participants

Safety, Tolerability and Pharmacokinetics of Multiple Rising Doses of BI 201335 NA in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2007-05-31

Completion:

2008-02-29

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182349 | COMPLETED | PHASE1

8 participants

Metabolism and Pharmacokinetics of Oral Solution of [14C]-BI 201335 in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2009-06-30

Completion:

2009-07-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182336 | COMPLETED | PHASE1

23 participants

Effects of BI 201335 NA on Cytochrome P450 and P-glycoprotein Activity Using a Probe Drug Cocktail in Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2008-06-30

Completion:

2008-09-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182323 | COMPLETED | PHASE1

74 participants

Safety, Tolerance, and Pharmacokinetics of Single Oral Doses of BI 201335 NA and Bioavailability in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2006-09-30

Completion:

2006-12-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182310 | COMPLETED | PHASE1

56 participants

Assessment of the Effect of BI 201335 on the QT Interval in Healthy Female and Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2008-06-30

Completion:

2008-10-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182297 | COMPLETED | PHASE1

50 participants

Safety, Tolerability, and Pharmacokinetics of BI 201335 NA in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2008-04-30

Completion:

2008-12-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182284 | COMPLETED | PHASE1

34 participants

Bioavailability of Soft Gelatin Capsule Formulation of BI 201335 NA Compared to the Solution Formulation in Healthy Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2008-01-31

Completion:

2008-02-29

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182271 | TERMINATED | PHASE1

8 participants

Single Rising Dose Study of BI 201335 ZW in Healthy Male Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2004-10-31

Completion:

2004-10-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182258 | COMPLETED | PHASE1

30 participants

Safety and Tolerability Study of BIBF 1120 as Intravenous Infusion and Absolute Bioavailability of BIBF 1120 as Soft Gelatine Capsule in Healthy Subjects

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2009-06-30

Completion:

2009-08-31

Conditions

• Healthy

Interventions

• DRUG

No Results Yet

NCT02182232 | COMPLETED | PHASE1

33 participants

A Dose Escalation Study of BIBF 1120 Together With Paclitaxel and Carboplatin in Patients With Advanced Stage Non-small-cell Lung Cancer

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2005-06-30

Completion:

2007-05-31

Conditions

• Carcinoma, Non-Small-Cell Lung

Interventions

• DRUG

No Results Yet

NCT02182206 | COMPLETED | PHASE1

50 participants

An Dose Escalation Study of Treatment With BIBF 1120 in Patients With Advanced Solid Tumours

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2003-06-30

Completion:

2005-06-30

Conditions

• Tumors

Interventions

• DRUG

No Results Yet

NCT02182193 | COMPLETED | PHASE1

54 participants

Safety and Relative Bioavailability of BIBF 1120 Soft Gelatine Capsules Charge 1, BIBF 1120 Soft Gelatine Capsules Charge 2 and BIBF 1120 Drinking Solution in Healthy Male Volunteers

Study Type:

INTERVENTIONAL

Last Updated:

2014-07-18

Start Date:

2006-09-30

Completion:

2006-11-30

Conditions

• Healthy

Interventions

• DRUG

No Results Yet