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NCT ID: NCT03030352 Completed - Child Development Clinical Trials

Promoting Children's Mental Health: The Effects of a Parenting Program

Start date: February 2014
Phase: N/A
Study type: Interventional

The objectives of the How-to parenting program are 1) to improve optimal parenting style, and 2) to foster children mental health (i.e. decrease in internalized and externalized problems, and well-being). The investigators expect that parents assigned to experimental groups will show improvements in parenting over time (i.e improvements in parental affiliation, parental structure and parental attitude toward autonomy), whereas parents in control groups will not show such improvements (i.e., stable or declining parenting quality). The investigators also expect children of parents in experimental groups to experience improvements in child mental health (i.e., fewer internalized and externalized psychological problems and increased well-being), whereas children whose parents are on the wait list will not show improvements over time (i.e., stable or deteriorating mental health and well-being).

NCT ID: NCT03029754 Completed - Intravenous Access Clinical Trials

Effect of Passive Leg Raise for Pediatric Peripheral IV Placement

Start date: May 17, 2017
Phase: N/A
Study type: Interventional

The investigators wish to determine whether passive leg raise allows for easier peripheral vascular access in the pediatric population. The investigators hypothesize that pediatric anesthesiologists will have higher rates of successful intravenous catheterization in children where a passive leg raise is employed.

NCT ID: NCT03029208 Completed - Anaemia Clinical Trials

Anemia Studies in Chronic Kidney Disease (CKD): Erythropoiesis Via a Novel Prolyl Hydroxylase Inhibitor (PHI) Daprodustat-in Incident Dialysis (ASCEND-ID)

Start date: May 11, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this multi-center study is to evaluate the efficacy and safety of daprodustat in subjects with anemia associated with CKD.

NCT ID: NCT03029143 Completed - Colitis, Ulcerative Clinical Trials

Vedolizumab Intravenous (IV) Dose Optimization in Ulcerative Colitis

ENTERPRET
Start date: March 29, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the efficacy and safety of vedolizumab intravenous (IV) dose optimization on mucosal healing compared with the standard vedolizumab IV dosing regimen over a 30 week treatment period in participants with moderately to severely active ulcerative colitis (UC) and high vedolizumab clearance, based on a Week 5 predefined serum vedolizumab concentration threshold less than (<) 50 microgram per milliliter (microg/mL) and who are Week 6 non-responders based on partial Mayo score.

NCT ID: NCT03028415 Completed - Clinical trials for Arthrodesis Surgery Involving the Hindfoot or Ankle

AMPLEX Ankle Fusion and Hindfoot

Start date: July 28, 2017
Phase: N/A
Study type: Interventional

To demonstrate that AMPLEX is non-inferior to autogenous bone graft (ABG) for bone fusion in a population indicated for single, double, or triple hindfoot arthrodesis or ankle arthrodesis surgery with supplemental graft material.

NCT ID: NCT03028363 Completed - Acne Vulgaris Clinical Trials

A Study of Olumacostat Glasaretil Gel in Subjects With Acne Vulgaris

Start date: December 27, 2016
Phase: Phase 3
Study type: Interventional

The objectives of this study are to assess the safety and efficacy of Olumacostat Glasaretil Gel compared to vehicle in patients with acne vulgaris

NCT ID: NCT03026959 Completed - Mindfulness Clinical Trials

Mindfulness and Maternal Mental Health

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

There is preliminary empirical support for the use of mindfulness interventions during the perinatal period; suggesting that mindfulness training may be an effective treatment approach for reducing depression and anxiety symptoms during pregnancy and reducing anxiety, stress, and psychological distress during the postpartum period. To extend on these findings, the purpose of this research is to evaluate the effectiveness of a brief mindfulness-based program in protecting maternal mental health and well-being using a randomized controlled trial.

NCT ID: NCT03026764 Completed - Osteoarthritis Clinical Trials

Inpatient vs Outpatient Total Hip Replacement

Start date: May 2015
Phase: N/A
Study type: Interventional

This study is a pragmatic randomized clinical trial comparing standard inpatient total hip arthroplasty with same day discharge. Patients who are medically well and have a good support structure at home will be randomized to inpatient or same day discharge. The investigators will compare patient costs from the perspective of the Ministry of Health, the institution, society and the patient. The investigators will also record complications, patient satisfaction, functional ability and quality of life.

NCT ID: NCT03026400 Completed - Clinical trials for Patient Satisfaction

Sub vs Trans-umbilical Incision: A Patient's Satisfaction-centered Trial

Start date: August 2014
Phase: N/A
Study type: Interventional

While some studies have suggested that subumbilical and transumbilical incisions have a similar clinical efficiency and safety, no study has yet evaluated their respective impact on patient's postoperative aesthetic satisfaction. The objective of this randomised trial is to compare patient's postoperative aesthetic satisfaction depending on the type of incision which is performed during surgeries.

NCT ID: NCT03026257 Completed - Myopia Clinical Trials

Clinical Assessment of a HYDRAGLYDE® Regimen

Start date: February 13, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate worn AIR OPTIX® plus HYDRAGLYDE® (AOHG) lenses cleaned and disinfected with HYDRAGLYDE® containing lens solutions compared to each of the control habitual silicone hydrogel (SiHy) lenses cleaned and disinfected with habitual multi-purpose solution (MPS) for cholesterol uptake.