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Signs and Symptoms clinical trials

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NCT ID: NCT02889536 Completed - Hernia Clinical Trials

Living With a Parastomal Bulge - a Phenomenological-hermeneutic Study of Patients Lived Experiences

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

A parastomal bulge (PB) is a frequent long-term complication after stoma formation. Most parastomal bulging occurs within two years of stoma formation but is seen up to 20 years post-surgery. A bulge may be relatively obvious or extremely difficult to diagnose, and descriptions of symptoms vary from 'asymptomatic', 'symptomatic' to 'high symptom load'. Previous studies report that quality of life as well as physical, psychological and social function are affected in patients with parastomal bulging. However, there is a lack of knowledge of patients' lived experiences with parastomal bulging. Insight into patients' experiences of symptoms in relation to parastomal bulging and the impact on everyday life may help identify issues of importance from the patient perspective. This, in turn, may help professionals to better understand and support patients with PB, and be of help when identifying patients' symptoms and determining relevant treatment strategies.

NCT ID: NCT02826408 Completed - Signs and Symptoms Clinical Trials

Effect of Proton Pump Inhibitors on Palpitations

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

Palpitation is a common complaint. Patients frequently feel this symptom despite having normal rhythm during symptoms. I have seen many patients who improve significantly on treatment with proton pump inhibitors (PPI). It may be that gastritis provokes a feeling of discomfort that subsequently starts the feeling of palpitation. On searching literature I found no study that investigated the effect of PPI's on palpitations. Therefore I propose a study where the investigators randomize people with palpitations with normal heart rate (no arrhythmia) and no apparent cause such as anxiety or clear illness to receive either PPI or placebo. The result will help to investigate if the improvement is true and if the results are positive this can provide a simple treatment for a common problem.

NCT ID: NCT02824692 Not yet recruiting - Clinical trials for Congestive Heart Failure

Preoperative Significant Clinical Findings Using Focused Ultrasound Examination

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

The purpose of this study is to determine whether a focused ultrasound examination for the heart, lungs and abdomen, preformed by a trained anesthesiologist, can reveal significant clinical findings in elderly patients before emergent surgery.

NCT ID: NCT02769559 Completed - Quality of Life Clinical Trials

Reduction Mammaplasty and Improved Quality of Life

MammaRed
Start date: January 2000
Phase: N/A
Study type: Observational

The data gathered here will be used to evaluate the efficacy and safety of the mammary reduction in patients with macromastia.

NCT ID: NCT02768311 Active, not recruiting - Clinical trials for Pain, Postoperative Pain Pathologic Processes Postoperative Complications Signs and Symptoms

Comparative Evaluation of Post Endodontic Pain Following Root Canal Treatment With Two Rotary System: Neolix & Waveone

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

Today, dentists tend to use rotary systems. Despite the increasing diversity of these systems as well as a few studies on the prevalence of pain after root canal treatment by rotary systems, And in particular, comparing the amount of pain after treatment, between systems RECIPROCAL AND FULL ROTATION single-file, the aim of this study was to evaluate the effect of applying canal preparation by the system, Neolix and WaveOne, on the prevalence of pain after endodontic treatments.

NCT ID: NCT02689817 Withdrawn - Pressure Ulcer Clinical Trials

Monitoring Physiologic Data in the Development of Pressure Ulcers

Start date: October 2019
Phase: N/A
Study type: Interventional

Hospital-acquired pressure ulcers (HAPUs) are a well-established serious complication of hospitalization that have serious consequences on patient morbidity and mortality as well as the cost of care. At the core of the problem for patient-centered targeted prevention of HAPUs is the lack of knowledge surrounding the magnitude and duration of pressure necessary to cause pressure ulcers, and the lack of immediate feedback on whether these interventions do anything to substantially offload at risk areas. Previous studies have been inconsistent in their findings of an association between duration of time and HAPU occurrence. While retrospectively this has been investigated, there is currently no substantial prospective, randomized study. This study seeks to better understand the interface pressures between the patient and his or her support surface and how this relates to the development of pressure ulcers. The effect of patient characteristics and the relationship between total length of time on the operating table and pressure ulcer development will also be assessed. The findings from this study will significantly add to strengthening the body of evidence regarding pressure ulcer development, specifically the relationship between the magnitude of interface pressure between the patient and the support surface for what duration of time leads to the development of a pressure ulcer. The results will provide critical insight into the physiologic targets healthcare providers should use to develop better pressure ulcer prevention programs, which could ultimately lead to a reduction in the incidence of pressure ulcers.

NCT ID: NCT02677090 Completed - Clinical trials for Signs and Symptoms, Digestive

Fiber Tolerability in Children Aged 3-7 Year

Fiber - TIC
Start date: January 2016
Phase: N/A
Study type: Interventional

Determination of the digestive tolerability of the PROMITOR® in children from 3 to 7 years old.

NCT ID: NCT02662699 Recruiting - Anemia Clinical Trials

Clinical Signs and Symptoms of Anemia in Patients Over 75 Years

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

Anemia is a common pathology in geriatrics. According to the World Health Organization it affects 23.9% of subjects over 60 years in the world, and 8% of patients over 60 years in Europe. A prevalence that increases with the age and twice in individuals over 85 years.

NCT ID: NCT02607293 Completed - Clinical trials for Polycystic Ovary Syndrome

A Study to Explore Correlation Between Symptoms and Signs of Polycystic Ovarian Syndrome (PCOS) and Risk of Over-response to Ovarian Stimulation

ARTIST
Start date: December 31, 2015
Phase:
Study type: Observational

This is a Phase IV, prospective, observational, single arm, multicenter trial to identify the population at high risk of overstimulation associated with signs and symptoms of PCOS and examines the utility of 12.5 international units (IU) increment of Gonal-f® new pen for individualized controlled ovarian stimulation (iCOS).

NCT ID: NCT02538601 Completed - Clinical trials for Post Traumatic Stress Disorder

Enhanced Smoking Cessation Intervention for Smokers Exposed to the World Trade Center (WTC) Disaster

Start date: February 2012
Phase: N/A
Study type: Interventional

The purpose of this study was to test the efficacy of a CBT-based smoking cessation treatment enhanced with transdiagnostic skills for the management of anxiety and fear-based avoidance behaviors (CBT-A) relative to a standard CBT-based smoking cessation treatment (CBT-S) for smokers with elevated PTSD symptoms who were exposed to the 9/11 World Trade Center disaster. The investigators hypothesized that the CBT-A treatment would yield more favorable outcomes with regard to smoking abstinence as well as improvements in PTSD and respiratory symptoms over a 6-month follow-up period.