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Active clinical trials for "Syndrome"

Results 8391-8400 of 9759

Risk Factors and Prognosis of Adverse Cardiovascular and Kidney Events After Coronary Intervention...

Cardio-Renal SyndromeCoronary Angiography3 more

As a single center, retrospective observation study in Guangdong Institute of Cardiovascular Diseases, this study included the main study population of patients who underwent coronary angiography and / or coronary intervention from January 2007 to Decemeber 2018. The hospitalization information was collected in the form of direct derivation of the case, and cardiac and renal adverse events were collected through outpatient recorder system. All-cause death information was obtained from the Public Security and matched to the electronic Clinical Management System of the Guangdong Provincial People's Hospital records.

Completed2 enrollment criteria

ARCANGELO (itAlian pRospective Study on CANGrELOr)

Acute Coronary Syndrome

The Sponsor implemented a post-authorisation safety study (PASS), category 3, focused in Acute Coronary Syndrome, in order to collect information about the safety of cangrelor in the real clinical practice, evaluating the safety of the transition to all the oral P2Y12 inhibitors (cangrelor, ticagrelor and prasugrel).

Completed9 enrollment criteria

Impact of Time-Restricted Eating on Metabolic and Neuroendocrine Homeostasis, Inflammation and Oxidative...

Metabolic SyndromeOverweight or Obesity3 more

The main purpose of the clinical trial is to determine the health impact of a dietary intervention known as time-restricted eating (TRE) in patients with metabolic syndrome (defined as the presence of elevated fasting plasma glucose and two or more of the following criteria: increased waist circumference, elevated fasting plasma triglycerides, reduced high-density lipoprotein-cholesterol, elevated blood pressure) and self-reported dietary intake of ≥14 hours per day. Participants will reduce the amount of time they eat to 10 hours per day over a 12-week monitored intervention followed by a 12-week self-directed intervention and will log their dietary intake using a smartphone application (myCircadianClock (mCC) app). Glucose homeostasis (blood glucose levels will be monitored continuously for 2 weeks at the baseline, at the end of the monitored intervention, and at the end of the self-directed intervention using a continuous glucose monitor), and other metabolic, neuroendocrine, inflammatory and oxidative stress/antioxidant defense biomarkers, body weight and composition, blood pressure, heart rate, sleep and activity (using mCC app), personal sense of wellness and dietary timing (using health questionnaires) will be evaluated at the baseline, at the end of the monitored intervention, and at the end of the self-directed intervention.

Unknown status21 enrollment criteria

Effect and Tolerance of a Probiotic-based Medical Device Administered to Patients With Irritable...

Irritable Bowel Syndrome

This is an observational, open, longitudinal, multicentre study conducted in France. The study plans to enrol 119 patients with irritable bowel syndrome who will be included by about 50 general practitioners or gastroenterologists consulting in private offices. The treatment, Lactiplus® is a medical device, in the form of capsules containing L. gasseri LA806. The main objective of the study is to assess the effect of a 4-week treatment with the medical device on abdominal pain.

Completed9 enrollment criteria

Effects of Progressive Muscle Relaxation Exercises During Pregnancy

Restless Legs Syndrome

Participants were allocated into three groups; the control group, progressive muscle relaxation (PMR) group and relaxation music (RM) group. The PMR and RM programs were explained toall participants, and the first program was tested under the supervision of the researcher. PMR and RM group participants performed the program daily throughout 4 weeks. Severity of RLS with the International Restless Leg Syndrome Scale (IRLSS) and sleep quality with the Pittsburgh Sleep Quality Index (PSQI) were assessed at baseline, 2 and 4 weeks for all the groups.

Completed13 enrollment criteria

Stellate Ganglion Block to Treat Long COVID 19 Case Series

Long COVIDLong Covid1913 more

An assessment of the effectiveness of Stellate Ganglion Block in alleviating symptoms of Long COVID-19.

Completed3 enrollment criteria

Thyroid Function and Structure IN Klinefelter Syndrome

Klinefelter SyndromeThyroiditis2 more

This is a longitudinal retrospective study for the evaluation of thyroid function and structure in patients with Klinefelter syndrome compared to healthy controls and patients affected by chronic lymphocytic thyroiditis.

Completed7 enrollment criteria

Psychological Risk Factors for Functional Somatic Disorders

Irritable Bowel SyndromeFibromyalgia5 more

The objective of this study is to explore the role of neuroticism, perceived stress, and adverse life events, respectively, in the development and perpetuation of functional somatic disorders.

Completed4 enrollment criteria

The Relationship Between Adipokines, Obesity and Insulin Resistance in Women With Polycystic Ovarian...

Polycystic Ovarian Syndrome

To evaluate possible clinical effects of adipokines , ( ghrelin, resistin and adiponectin), in obese and non-obese patients with polycystic ovary syndrome (PCOS).

Completed4 enrollment criteria

VitalScan MCG Rule-out Multi-centre Pivotal Study - UK

Acute Coronary Syndrome

The study is a prospective multi-centre observational study to evaluate a portable magnetocardiograph device for the rule-out of acute coronary syndrome (ACS) in patients who present to the emergency department with chest pain and other symptoms consistent with ACS.

Completed14 enrollment criteria
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