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NCT ID: NCT02735421 Completed - Acne Vulgaris Clinical Trials

Adapalene 0.3% - Benzoyl Peroxide 2.5% Gel and Risk of Formation of Atrophic Acne Scars

OSCAR
Start date: May 13, 2016
Phase: Phase 4
Study type: Interventional

This was a multi-centre, randomized, investigator blinded, vehicle controlled trial using intra-individual comparison (right half-face versus left half-face). Participants with each half-face randomized to one of the two following treatments: - Adapalene 0.3 percent (%) - benzoyl peroxide (BPO) 2.5% gel (TactuPump® Forte). - Vehicle gel The main objective of this trial was to evaluate the effect of Adapalene 0.3% - BPO 2.5% (ABPO Forte) gel versus vehicle gel on the risk of formation of atrophic acne scars in moderate to severe acne participants.

NCT ID: NCT02735044 Completed - Clinical trials for Type 1 Diabetes Mellitus

Comparison of the Safety and Efficacy of HOE901-U300 With Lantus in Children and Adolescents With Type 1 Diabetes Mellitus

EDITION JUNIOR
Start date: April 14, 2016
Phase: Phase 3
Study type: Interventional

Primary Objective: To compare the efficacy of a new formulation of insulin glargine (HOE901-U300) to Lantus in terms of change of HbA1c from baseline to endpoint (month 6) in children and adolescents with type 1 diabetes mellitus. . Secondary Objectives: To compare HOE901-U300 and Lantus in terms of: - Percentage of participants reaching target HbA1c and fasting plasma glucose (FPG). - To assess the safety of HOE901-U300 including analysis of events of hypoglycemia, events of hyperglycemia with ketosis, and development of anti-insulin-antibodies.

NCT ID: NCT02734862 Completed - Fungal Infection Clinical Trials

CD101 Compared to Caspofungin Followed by Oral Step Down in Subjects With Candidemia and/or Invasive Candidiasis-Bridging Extension

STRIVE
Start date: July 26, 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if intravenous CD101 is safe and effective in the treatment of candidemia and/or invasive candidiasis when compared to caspofungin (followed by oral fluconazole).

NCT ID: NCT02734706 Completed - Clinical trials for Hypercholesterolemia

Efficacy of a LRC™ (L. Reuteri NCIMB 30242) Capsule on Managing Cholesterol in Adults

Start date: March 2016
Phase: N/A
Study type: Interventional

To investigate the effect of a supplement capsule containing LRC™ (L. reuteri NCIMB 30242), taken twice daily with lunch and dinner (NLT 2.5E9 CFU per dose), versus placebo capsule on serum low density lipoprotein (LDL)-cholesterol in otherwise healthy hypercholesterolemic adults after 9 weeks of product consumption.

NCT ID: NCT02734173 Completed - Hepatitis C Clinical Trials

Pilot HCV Direct Acting Antiviral Therapy and Metabolism

3D
Start date: July 2015
Phase: Phase 4
Study type: Interventional

There is compelling data supporting the pursuit of research into the effects of HCV antivirals on metabolic homeostasis. As a further rationale and justification, the experience with HIV antiretrovirals has clearly demonstrated that antiviral medications can produce profound changes in glucose metabolism, lipid profile and other measures of metabolic homeostasis. This establishes biological plausibility for this focus of research in HCV. The new knowledge created from this research will: 1. Provide new information on the metabolic effects of the Abbvie 3D HCV antiviral regimen. 2. Provide insight as to whether there are metabolic advantages with RBV-free compared to RBV-containing HCV regimens. This is particularly relevant given the current uncertainty regarding the need for RBV in IFN-free, oral DAA regimens. 3. Provide insight into the impact of cirrhosis on metabolic milieu before, during and after HCV antiviral therapy

NCT ID: NCT02734121 Completed - Breast Cancer Clinical Trials

PEGI to Improve Shared Decision-Making for Breast Reconstruction

PEGI
Start date: February 15, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of a pre-consultation decision support workshop for breast reconstruction after breast cancer, in facilitating the decision-making process, compared to routine pre-surgical education.

NCT ID: NCT02733250 Completed - Lung Cancer Clinical Trials

Pembrolizumab With Nab-Paclitaxel in Non-Small Cell Lung Cancer

URCOH-PMS-001
Start date: March 13, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the optimal dose of nab-paclitaxel to be safely administered in combination with pembrolizumab in patients with advanced inoperable non-small cell lung cancer. The study is also aimed at evaluating the efficacy of the combination therapy.

NCT ID: NCT02732847 Completed - Clinical trials for Acute Upper Respiratory Tract Infections

Trial of Post-Dated Delayed Antibiotic Prescriptions

Start date: October 2007
Phase: N/A
Study type: Interventional

Delayed prescriptions have been shown to lower antibiotic use for upper respiratory tract infections (which are mostly viral). This trial will test the hypothesis that if the clinician post-dates the delayed prescription by 2 days, rather than dating it on the day the patient is seen, there will be a further drop in the rate of antibiotic use.

NCT ID: NCT02732210 Completed - Clinical trials for Osteoporosis, Age-Related

Persistence With Prolia® (Denosumab) in Postmenopausal Women With Osteoporosis

Start date: July 6, 2011
Phase:
Study type: Observational

The objective of this study was to describe persistence with Prolia® 60 mg administered subcutaneously (SC) every 6 months (Q6M) at 12 and 24 months.

NCT ID: NCT02732184 Completed - Clinical trials for Acute Myeloid Leukemia

A Multiple Dose, Dose Escalation Trial of AEB1102 in Patients With AML or MDS

Start date: August 2016
Phase: Phase 2
Study type: Interventional

This is the first study of the safety of increasing dose levels of AEB1102 in patients with Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome. The study will also evaluate the amounts of AEB1102 in blood, the effects of AEB1102 on blood amino acid levels and the antitumor effects of AEB1102.