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NCT ID: NCT04289012 Completed - Clinical trials for STEMI - ST Elevation Myocardial Infarction

HELicobacter Pylori Screening in Patients With Acute Myocardial Infarction Pilot Study

HELPpilot
Start date: November 7, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to determine the prevalence of Helicobacter pylori (Hp) infection in patients with myocardial infarction (MI). This is performed to establish the feasibility of a large trial examining whether systematic screening for and subsequent eradication therapy significantly reduces the risk of hospitalization for upper gastrointestinal (GI) bleeding in patients after MI.

NCT ID: NCT04284072 Completed - Epilepsy Clinical Trials

Clinical Scenarios for Long-term Monitoring of Epileptic Seizures With a Wearable Biopotential Technology

SeizeIT2
Start date: June 22, 2020
Phase: N/A
Study type: Interventional

Clinically validate a biopotential and motion recording wearable device (Byteflies Sensor Dot) for detection of epileptic seizures in the epilepsy monitoring unit (EMU) and at home.

NCT ID: NCT04281368 Completed - Intra-Uterine Death Clinical Trials

Analysis of All Stillbirths in Stockholm County 2017, a Multidisciplinary Audit

Start date: June 1, 2019
Phase:
Study type: Observational

All stillbirths in Stockholm during 2017 were analysed according to the primary outcomes which were preventable/non-preventable deaths and the level of delay. The secondary outcomes were: causes of death, standard of care pre and post stillbirth and if a summary of the possible causes of death was made as well as the planning of supervision of the next pregnancy.

NCT ID: NCT04281043 Completed - Quality of Life Clinical Trials

Quality of Life After Robotic Surgery for Endometrial Cancer

QoL
Start date: June 15, 2019
Phase:
Study type: Observational

The purpose of this study is to investigate how robotic assisted laparoscopic surgery affects the quality of life of women who are treated with primary surgery for endometrial cancer. So far, very little has been published and basically no long-term follow-up. Included patients respond to questionnaires preoperatively, 2 weeks after surgery and 3 months and 12 months after surgery. Each patient thus answers the questionnaires (the same) on four occasions. The questionnaires used are validated and used extensively internationally. The first survey has two parts, QLQ30 and the module for endometrial cancer EN24. In addition the study includes use PHQ -9 and GAD 7.

NCT ID: NCT04280731 Completed - Clinical trials for Microbial Colonization

Impact of Quinoa Milk Fermented With Lactic Acid Bacteria From Foods on Human Oral and Intestinal Flora

Start date: January 7, 2020
Phase: N/A
Study type: Interventional

The demand for alternatives to dairy products has increased in recent years and a lot of proposals for vegetable milk and yogurt products have taken place in the market. Quinoa is a plant from South America that has growth in popularity in recent years as many sought out nutritious and healthier eating, the herb is known for its high nutritional value. It is complete protein source containing all the essential amino acids. If this herb were fermented with probiotic bacteria, there is a potential for a product that is lactose free, gluten free and cholesterol free. The probiotic potential of quinoa milk, fermented with food associated lactic acid bacteria will be investigated. This includes a study that examines how daily consumption of this vegetable drink changes the composition of the oral and intestinal flora. Therefore, healthy people are now seeking to participate in the study, which will be for just over 2 weeks.

NCT ID: NCT04277793 Completed - Anxiety Clinical Trials

Feasibility Evaluation of a Monitored Self-guided Cognitive Behavioural Therapy Digital Format

Start date: April 24, 2020
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the feasibility of a new monitored self-guided digital cognitive behavioural therapy format through one of the key components of an intervention for depression and anxiety (Problem Solving) and to answer the question: Do patients with significant levels of depression and/or anxiety symptoms consider the monitored self-guided digital format usable and credible? An uncontrolled trial will explore participant's usability and treatment credibility ratings.

NCT ID: NCT04276584 Completed - Clinical trials for Postoperative Respiratory Complications

Effect of Speaking Aloud After Abdominal Surgery.

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

Hypoxia and reduced vital capacity is commonly occurring after abdominal surgery. Positive expiratory pressure is one treatment suggested to improve lung function after surgery. We aim to test whether speaking improves postoperative oxygen saturation and ventilation after abdominal surgery. In a cross-over design, 50 subjects will be randomized to start with either positive expiratory pressure maneuvers, i.e. deep inspiration followed by expiration in a positive expiratory pressure device at 10-15 cm of water, or to start with reading a text loudly. Arterial blood gases will be taken at study start. Patients will be monitored using Noxturnal T3, Res Med for respiration and pulse oximetry, and online transcutaneous carbon dioxide partial pressure measurements (SenTec Digital monitoring systems). Main outcome measurements include oxygen saturation after speaking compared with positive expiratory pressure therapy.

NCT ID: NCT04272112 Completed - Clinical trials for Dental Prosthesis Failure

Clinical Performance of All-ceramic Posterior Crowns. A Randomized, Prospective Clinical.

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

This is a randomized, prospective clinical trial. The aim of the project is to assess the clinical performance of three types of tooth-supported crowns; monolithic high translucent colored zirconia, crowns of high-translucent colored zirconia with a mini-veneer buccally and crowns of lithium-disilicate glass-ceramic. Crowns will be placed on posterior teeth and evaluated from an esthetic and functional point of view, to identify if there are any differences between the materials.

NCT ID: NCT04272047 Completed - Athletic Injuries Clinical Trials

Prevention of Lower Limb and Groin Injuries: the Sport Without Injury ProgrammE (SWIPE) Football Trial

SWIPEsoccer
Start date: March 30, 2020
Phase: N/A
Study type: Interventional

This is a three-armed intervention study that evaluates the injury preventive effects of three different training interventions in youth and adult football players. Two intervention arms are randomized and one arm acts as a non-randomized comparison group. Half of randomized participants will receive a general injury prevention exercise program with emphasis on the lower extremities, and the other half a hip/groin focused injury prevention exercise. A third group of participants who already use an injury prevention exercise program at study inclusion are invited to participate as a non-randomized comparison group and continue their usual training practices.

NCT ID: NCT04271683 Completed - General Anesthesia Clinical Trials

Safe Use of CPAP and PEEP During Induction of General Anesthesia

Start date: October 19, 2021
Phase: N/A
Study type: Interventional

The study compares the safety of using pressure controlled ventilation with a positive end-expiratory pressure (PEEP) during induction of general anaesthesia immediately after apnoea to a standard method starting ventilation manually without PEEP immediately after apnoea.