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NCT ID: NCT03703882 Completed - Clinical trials for Muscular Dystrophy, Duchenne

Phase III Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy

PolarisDMD
Start date: October 2, 2018
Phase: Phase 3
Study type: Interventional

The PolarisDMD study is a Phase 3, global study to evaluate the efficacy and safety of edasalonexent in pediatric patients with a genetically confirmed diagnosis of DMD. Male patients from 4-7 years of age (up to 8th birthday) will be enrolled. Edasalonexent is an orally administered small molecule that inhibits NF-kB, which is the key link between loss of dystrophin and disease pathology and plays a fundamental role in the initiation and progression of skeletal and cardiac muscle disease in DMD.

NCT ID: NCT03703024 Completed - Clinical trials for Osteoarthritis, Knee

An Intervention Study Evaluating the Effects of a Raspberry Leaf Extract in an Osteoarthritic Population.

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

A double-blind, randomized, placebo-controlled clinical study to evaluate the efficacy of raspberry extract to alleviate symptoms of osteoarthritis in the knee.

NCT ID: NCT03701113 Completed - Clinical trials for Osteoporosis, Postmenopausal

Milk Protein and Bone Health in Postmenopausal Women

OSTEOMILK
Start date: October 22, 2018
Phase: N/A
Study type: Interventional

The process of bone remodeling exhibits pronounced diurnal pattern that is important for bone health. A balanced rate of bone resorption is required to maintain bone health, a balance that can be disturbed during the life-cycle to effect net rate of formation (as occurs during growth and development to adulthood) or net resorption (as occurs, for example, during the menopause). Bone turnover is a nutritionally modulated process and the investigators believe a milk-based protein supplement (MBPS) can modulate beneficially the rate of bone resorption over the time period when bone remodeling is most active i.e. late evening/overnight. In this novel approach to the timing of nutrient ingestion, the proposed nutrient intervention seeks to modify (reduce) the rate of bone resorption and promote the rate of bone formation to the benefit of bone health in this at risk population..

NCT ID: NCT03699111 Completed - Clinical trials for Advanced Colorectal Cancer

Identification of New Patient Stratification Tools in MSS RAS mt mCRC

COLOSSUS
Start date: September 19, 2018
Phase:
Study type: Observational

This is a translational, multicentre and multinational study. The aim of this study is to identify new patient stratification tools in microsatellite stable RAS mutant metastatic Colorectal Cancer

NCT ID: NCT03698630 Completed - Asthma Clinical Trials

Single Dose Oral Dexamethasone Versus Multi-dose Prednisolone in the Treatment of Acute Exacerbations of Asthma in Children

Start date: July 6, 2011
Phase: Phase 4
Study type: Interventional

A trial to investigate if a single dose of the oral corticosteroid, Dexamethasone is as effective in treating exacerbations of asthma in children as 3 days of treatment with another oral corticosteroid, Prednisolone

NCT ID: NCT03695588 Completed - Clinical trials for Quadratus Lumborum Block

Quadratus Lumborum Block (QLB) for Pain Relief After Caesarean Section

Start date: October 30, 2018
Phase: N/A
Study type: Interventional

There is currently a gap in the literature with regards to the utility of the QLB performed in conjunction with intrathecal morphine (ITM) for Caesarean section. The aim of the study is to assess the efficacy of the QLB as part of a multi-modal analgesic approach in patients after caesarean section.

NCT ID: NCT03694509 Completed - Gastric Emptying Clinical Trials

Gastric Emptying After Tea With Milk in Pregnancy.

Start date: October 30, 2018
Phase: N/A
Study type: Interventional

The aim of the study is to assess the difference in gastric emptying using ultrasound of pregnant patients following a cup of tea with milk or a similar volume of water.

NCT ID: NCT03692806 Completed - Metabolic Syndrome Clinical Trials

Efficacy of STABLOR® on Visceral Fat Mass Reduction in Patients With Metabolic Syndrome

OBEMINALE2
Start date: September 11, 2018
Phase: N/A
Study type: Interventional

The primary objective of the study is to assess the efficacy of STABLOR® consumption on visceral fat mass compared to placebo, in persons with metabolic syndrome during 12 weeks of consumption.

NCT ID: NCT03691779 Completed - Cystic Fibrosis Clinical Trials

Evaluation of VX 445/TEZ/IVA in Cystic Fibrosis Subjects 6 Through 11 Years of Age

Start date: October 2, 2018
Phase: Phase 3
Study type: Interventional

This study will evaluate the pharmacokinetics (PK), safety, tolerability, efficacy, and pharmacodynamic effect of VX-445, tezacaftor (TEZ), and ivacaftor (IVA) when dosed in triple combination (TC) in Cystic Fibrosis (CF) subjects 6 through 11 years of age with F/F and F/MF genotypes.

NCT ID: NCT03688841 Completed - Varicose Ulcer Clinical Trials

Negative Pressure Vs. Compression in Venous Ulcers

Start date: January 19, 2016
Phase: N/A
Study type: Interventional

This study randomises patients with venous leg ulcers, to be managed either using conventional compression bandages or a bridged vacuum assisted closure system under compression.