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NCT ID: NCT03494452 Completed - Low Back Pain Clinical Trials

Trunk Muscle Strength, Strength Endurance and Activity in Persons With Low Back Pain

TRUSC
Start date: October 10, 2017
Phase:
Study type: Observational

The research questions are if persons with low back pain (LBP) have lower trunk muscle strength, lower trunk muscle strength endurance and lower trunk muscle activity than healthy controls and if functional limitations because of LBP are related to the level of muscle strength, strength endurance and activity. To investigate this investigators will carry out a clinical assessment including questionnaires and a biomechanical assessment comprising muscle strength tests, muscle strength endurance tests and electromyographic (EMG) analysis of selected trunk muscles.

NCT ID: NCT03494413 Completed - Cerebral Perfusion Clinical Trials

Transpharyngeal Doppler Sonography for Cerebral Perfusion Monitoring

TaPaS
Start date: July 10, 2018
Phase: N/A
Study type: Interventional

This prospective interventional study investigates transpharyngeal sonography (TPS) as an additional neuromonitoring strategy to assess cerebral perfusion during cardiovascular surgery. In the first part of the study the investigators will investigate the feasibility of TPS for visualization of aortic arch branches including the innominate and the carotid arteries in patients undergoing cardiac surgery with cardiopulmonary bypass. In the second part the investigators plan to adopt the investigators previous experiences on TPS to a selected population of patients undergoing ascending aortic and/or arch repair in hypothermic circulatory arrest (HCA).

NCT ID: NCT03494205 Completed - Clinical trials for Radiation Dermatitis

Urtica Comp. Gel for Prevention and Therapy of Radiation Dermatitis

Urticacomp
Start date: May 2, 2018
Phase: Phase 2
Study type: Interventional

A randomized controlled trial comparing Urtica comp. gel (Swissmedic listed medication in the category of "Anthroposophic Medication without Indication") against standard skin care, examining its effect in prevention and treatment of radiation dermatitis in breast cancer patients under Radiation therapy.

NCT ID: NCT03494101 Recruiting - Clinical trials for Salmonella Infection Non-Typhoid

Interaction Between Non-typhoid Salmonella, Host Microbiota, and Immune System During Acute Infection and Remission

Start date: June 15, 2018
Phase:
Study type: Observational

Stool and blood samples from patients with a non-typhoid Salmonella infection will be collected during an observation period of six months and analyzed for changes in the microbiota diversity and composition, mutation rates in the Salmonella strains and the specific immune response evoked by the infection. Findings are compared to healthy individuals and individuals with acute, infectious diarrhea caused by other microorganisms.

NCT ID: NCT03493399 Not yet recruiting - Craving Clinical Trials

Testing Interference-based Methods to Mitigate Gambling Craving - A Multiple Single Case Design

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Gambling craving is involved in the development, maintenance and relapse of gambling disorder. Yet, it lacks research regarding evidence-based interventions available to mitigate craving in patients displaying gambling disorder. The elaborated intrusion theory of desire (EIT) is a cognitive model of craving which offers important avenues for the development of psychological interventions, as it clearly describes the processes at play in craving experiences (e.g., mental imageries, working memory). Recent research evidenced that the elaborated intrusion theory is relevant to account for gambling craving experiences. According to this model, craving (and desire) is the result of an elaboration process where "desires thoughts" (mental images and thoughts), induced by internal (e.g., frustration) and/or external (e.g., advertisement) triggers, require attentional and cognitive resources. The principle of interference-based techniques is to move the resources allocated to the elaboration of intrusive desire thoughts to a competing task (e.g., clay modelling, competitive mental imagery, Tetris) in order to monopolize the resources underlying craving, thus preventing its elaboration and reducing its vividness and overwhelming nature. Several studies have shown the efficacy of such techniques to reduce substance-related craving. Yet, data obtained on clinical samples remain scarce. Preliminary data have been obtained prior to this application. In order to investigate the relevance of interference-based techniques, an experimental study was conducted in community gamblers. In two conditions (19 gamblers per condition), gambling craving was first induced via a short mental imagery session and a computer-generated gambling simulation task. Then, the experimental group was asked to perform an interference task consisting of creating a vivid mental image of a bunch of keys. The control group completed a task in which they had to pop and count bubble wrap. The analyses revealed that induced craving decreases significantly in both groups. However, participants that are considered problem gamblers showed a greater decrease of their craving in the experimental condition. This previous "proof of principle" study supports that interference-based techniques are potentially promising interventions to reduce craving in problem gambling. It also warrants further research as no data is available in clinical population. The current project consists in a pilot study aiming to test the efficacy of interference-based techniques in a sample of gambling disorder patients. The investigators decided to adopt a multiple single case design, as this methodology is ideal in the sense that it helps to understand the whole process of an interference-based intervention among a small number (10) of outpatients with a gambling disorder, without control group. Ecological Momentary Assessment will be used to allow intervention no naturally occuring craving. In addition to be easily implementable in a clinical design, this design will provide sufficient evidences before possibly, in a second time, further validation of these techniques using a randomized-control trial.

NCT ID: NCT03491579 Withdrawn - AML Clinical Trials

Epacadostat, Cladribine and Cytarabine (ECC) in AML

ECC
Start date: December 2018
Phase: Phase 1
Study type: Interventional

This trial assess the maximum tolerated dose (MTD) and to characterize dose-limiting toxicities (DLTs) of epacadostat when added to the cladribine/cytarabine chemotherapy in relapsed / refractory AML patients fit for intensive treatment

NCT ID: NCT03491462 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Arimoclomol in Amyotropic Lateral Sclerosis

Start date: July 31, 2018
Phase: Phase 3
Study type: Interventional

A multicenter, randomized, double-blind, placebo-controlled, parallel group trial to evaluate the efficacy and safety of arimoclomol in amyotropic lateral sclerosis (ALS)

NCT ID: NCT03490630 Recruiting - Anesthesia Clinical Trials

Patient Reported Outcome After Bariatric Surgery

Start date: January 2011
Phase:
Study type: Observational

Prospective association study to analyse patients' outcome after bariatric surgery. Outcome comprises postoperative pain, analgesia, postoperative side-effects, long-lasting pain, patients' impairment in daily living.

NCT ID: NCT03490175 Completed - Anesthesia Clinical Trials

Genetic Variants and Non-genetic Variables and Postoperative Nausea and Vomiting

Start date: January 2011
Phase:
Study type: Observational

Prospective observational study to analyse the association of non-genetic variables as well as genetic variants of candidate genes with the incidence of postoperative nausea and vomiting (PONV).

NCT ID: NCT03489499 Recruiting - Postoperative Pain Clinical Trials

Genetic Variants and Postoperative Pain

Start date: January 2011
Phase:
Study type: Observational

Prospective observational study to analyse patients' pain related outcome after surgery and ist association to genetic variants and non-genetic variables.