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NCT ID: NCT03215641 Enrolling by invitation - Pediatric Obesity Clinical Trials

Is it Helpful to Use Fitbits in a Family Based Weight Loss Program?

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

This study evaluates the role of personal activity trackers to help improve weight loss or weight maintenance for children and their parents enrolled in a comprehensive weight loss program.

NCT ID: NCT02681770 Enrolling by invitation - Clinical trials for Kidney Transplantation

Individual and Dyadic Functioning, Adherence, and Quality of Life After Kidney Transplantation

IDyAL
Start date: August 2016
Phase: N/A
Study type: Observational

Following solid organ transplantation, adherence to treatment regime (especially with regard to a reliable intake of immunosuppressant medication) is crucial for transplant survival, and has an impact on the patients' health and morbidity. Approximately 35 % of graft rejection or failure cases in kidney transplant patients are due to insufficient levels of adherence or non-adherence to immunosuppressant medication. Adherence is influenced by both individual and interpersonal aspects in complex interaction. This study aims at investigating individual and dyadic functioning of both patients and their spouses following kidney transplantation. Outcome measures of interest are patient's level of adherence and both patient and spouse's subjective quality of life.

NCT ID: NCT02729623 Enrolling by invitation - Healthy Clinical Trials

The Pharmacokinetics, Safety, and Ease of Use of a Portable Metered-Dose Cannabis Inhaler

Start date: August 2016
Phase: Phase 1
Study type: Interventional

Growing evidence supports the use of inhaled cannabis for neuropathic pain; the lack of standard inhaled dosing holds a major obstacle in cannabis becoming a pharmacological treatment for neuropathic pain. The objective of this study is to explore the pharmacokinetics, safety, tolerability, and ease of use of a portable metered-dose inhaler, (i.e. CannaHALER) for cannabis in a cohort of 12 healthy volunteers. In a single escalating dose methodology, open-label study, patients will inhale a single 10 ± 0.1 mg / 15 ± 0.1 mg / 20 ± 0.1 mg / 25 ± 0.1 mg dose of cannabis using the Kite Systems cannaHALER cannabis Inhaler device. Blood samples will be taken at baseline and up to 30 minutes. Adverse events will be monitored following the inhalation.

NCT ID: NCT02873455 Enrolling by invitation - Colorectal Cancer Clinical Trials

Effects of Video Information on Preoperative Anxiety in Patients With Colorectal Cancer

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

Patient's anxiety prior to surgery has been linked to more harmful outcome after surgery. The investigators aim to evaluate the effect of video information on preoperative anxiety level in patients with colorectal cancer.

NCT ID: NCT02894229 Enrolling by invitation - Clinical trials for Stress, Psychological

The Stress Reduction Intervention Study

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

The primary purpose of the present study is to investigate the relationship between mindfulness and stress habituation. The investigators propose to measure the effect of mindfulness on stress habituation by randomly assigning participants to a 6-week mindfulness-based stress reduction group intervention, a cognitive-behavioral skills group comparison intervention, or a waitlist control condition followed by repeated acute psychosocial stress testing (2 laboratory sessions on 2 separate days). Saliva will be collected from participants throughout both laboratory testing sessions to measure HPA axis activation (an essential stress-responsive system), along with other measures of physiological and psychological stress (e.g., heart rate, blood pressure, emotions). Mediators and moderators of treatment outcome will be examined. The cognitive-behavioral skills group condition is an appropriate comparison group due to the well-documented efficacy of cognitive-behavioral interventions on stress.

NCT ID: NCT02895191 Enrolling by invitation - Clinical trials for Acute Respiratory Distress Syndrome

The Safety and Dose Response Relationship of Ulinastatin for Acute Respiratory Distress Syndrome(ARDS)

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

Compared with placebo, evaluate the effects and safety of Ulinastatin(UTI) added to conventional treatment for ARDS; Evaluate the dose response relationship of Ulinastatin for ARDS.

NCT ID: NCT02895685 Enrolling by invitation - Clinical trials for Technical Skills Training

Group Dynamics in Surgical Skill Training

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

The investigators have planned a randomized study, examining the effect of self-directed training in groups vs. individual training on trainees' acquisitions of open surgical skills. Eighty participants who signed up for a pre-existing simulation-based course in basic open surgical skills will be randomized to practice either in pairs or individually during the course. Participants open surgical skills will be tested on a simulated skin model before and after the course. The investigators hypothesis is that dyad training will enhance self-directed learning in open surgical skills.

NCT ID: NCT02934776 Enrolling by invitation - Clinical trials for Magnetic Resonance Imaging

Prospective Cohort Study of the Ability of MRI/DTI to Diagnose Prostate Cancer

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

The purpose of this study is to examine if investigators can improve diagnosis of prostate cancer by using MRI/DTI?

NCT ID: NCT02949050 Enrolling by invitation - Rhinitis Clinical Trials

Corn Occupational Rhinitis SCIT Efficacy Study

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

Patients demonstrated allergic to corn pollen and timothy grass pollen (by allergy testing) who have undergone 1 to 2 years of subcutaneous allergen immunotherapy (SCIT) containing timothy grass extract with moderate symptomology (as documented via rhinitis symptom score surveys) will constitute the treatment group. Those who previously chose not to undergo SCIT who have documented symptomology and are skin test positive to corn pollen will constitute the control group. Prospective symptom score analyses and retrospective quality of life assessments (RQLQ) will be the primary and secondary efficacy outcome measures.

NCT ID: NCT03141112 Enrolling by invitation - Severe Sepsis Clinical Trials

The Benefits of Early Initiation of Continual Renal Replacement Therapy in Patients With Severe Sepsis

Start date: August 2016
Phase: N/A
Study type: Observational

The study will evaluate the benefit of early initiation of CRRT in the initial phase of severe sepsis in patients admitted to the ICU. Primary evaluated end-point is 28-day mortality. Secondarily evaluated end-point is length of ICU-stay, length of stay in hospital, duration of mechanical ventilation. There are two groups. One group of participants with early CRRT initiation and another group with late CRRT initiation. Reference group no CRRT.