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NCT ID: NCT03875430 Not yet recruiting - Menopause Clinical Trials

Study to Investigate the Effectiveness of a Food Supplement Made of Hop in the Improvement of Menopausal Symptoms

OLSEM
Start date: April 15, 2019
Phase:
Study type: Observational

This observational study will assess the effects of a dietary supplement based on Humulus Lupulus L. to relieve the symptoms of menopause in perimenopausal and postmenopausal women, by doing a follow up of the Cervantes scale and the Anxiety and depression Goldberg Scale in a period of 6 months. Participants will be allocated to dietary supplement being the difference between groups if they are perimenopausal or postmenopausal, and will attend to 3 visits (baseline, 3 months and 6 months).

NCT ID: NCT03899714 Not yet recruiting - Cryotherapy Clinical Trials

Return to Physical Activity Following Injury: Towards Understanding a More Accessible Solution for Shorter Recovery Time.

Start date: April 15, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of cryotherapy application on hip adductors and ankle evertors on the Overall Stability Index (OSI), the Medio-Lateral Stability Index (MLSI), and the Antero-Posterior Stability Index (APSI) in healthy adult females.

NCT ID: NCT03902769 Not yet recruiting - Clinical trials for Acute Myeloid Leukemia

Study to Assess Length of Remission With Intensive Chemotherapy in Rapidly Responding AML Patients.

AML
Start date: April 15, 2019
Phase: N/A
Study type: Interventional

We previously reported results of a prospective observational study demonstrating that early response defined as reduction in bone marrow (BM) blast counts to less than 5% of BM cells by the fifth day of induction therapy is a strong predictor of remission and overall survival (Ofran Y, et al. AJH, 2015). The long term survival benefit of early response was confirmed later on after a median follow-up for surviving patients of 53 months (range 17.5-84.5).

NCT ID: NCT03910829 Not yet recruiting - Chronic Pain Clinical Trials

Effects of Motor Imagery and Action Observation Training on Neck Reposition Sense in Patients With Chronic Neck Pain

Start date: April 15, 2019
Phase: N/A
Study type: Interventional

This study evaluates the influence of motor imagery or action observation training on joint position error in patients with chronic neck pain. This variable is a measure of proprioception and cervical motor control. A group of patients will receive an action observation training of neck movements, another will receive a protocol of motor imagery of the same movements and the last group will be a placebo group, through the viewing of a documentary video.

NCT ID: NCT03284294 Not yet recruiting - Schizophrenia Clinical Trials

Influence of Vitamin D Supplementation on Serum BDNF Level and Cognitive Function in Schizophrenia

Start date: April 15, 2020
Phase: Phase 3
Study type: Interventional

The objective of the study is to evaluate the influence of vitamin D supplementation on Serum Brain Derived Neurotrophic Factor level and cognitive function in schizophrenia treated with atypical antipsychotic. Methods: The investigator will use randomized controlled trial design. 40 chronic schizophrenia patients with vitamin D insufficiency or deficiency treated with atypical antipsychotic, will be randomly assign (1:1 ratio) to receive either daily oral cholecalciferol 2000 IU or placebo for 8 weeks. Assessment of BDNF serum and cognitive function will be performed at baseline and after 8 weeks period.

NCT ID: NCT03905109 Not yet recruiting - Crohn Disease Clinical Trials

Safety Evaluation of ABX464 in Patients With Moderate to Severe Active Crohn's Disease

Start date: April 15, 2020
Phase: Phase 2
Study type: Interventional

This Phase IIa study is a 16-week, double-blind, placebo-controlled, randomized study aiming at evaluating the safety and the efficacy of ABX464 given once a day (o.d) at 50 mg in subjects with moderate to severe active Crohn's Disease who have inadequate response, loss of response, or intolerance to prior amino-salicylates, immunosuppressant treatment, biologics, and/or corticosteroid treatment, and followed by a 4 weeks period of follow-up after the last study drug intake.

NCT ID: NCT04140370 Not yet recruiting - Frailty Clinical Trials

Frailty Prevalence in Surgical European Patients. European Prospective Cohort Stufy of the Prevalence of Frailty in Surgical Patients.

FRAGILE
Start date: April 15, 2020
Phase:
Study type: Observational [Patient Registry]

European prospective one day cohort study. Analysis of the prevalence of frailty and predefined 30-day postoperative complications in adult patients undergoing emergency or elective surgery.

NCT ID: NCT04174898 Not yet recruiting - Aging Well Clinical Trials

MSC Infusion for Anti-aging and Regenerative Therapy

REGEN
Start date: April 15, 2020
Phase: Phase 1
Study type: Interventional

To evaluate the safety and efficacy of human Mesenchymal Stem Cell (hMSC) infusion therapy, in preserving general wellness and ameliorating or reversing the effects of aging in our study population

NCT ID: NCT04306627 Not yet recruiting - Clinical trials for Hypercholesterolemia

Effect of Atorvastatin on Carotid Intima Media Thickness

Start date: April 15, 2020
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that additive effects of combined antihypertensive medications and statin in a single pill combination may better reduce progression of vascular remodeling and inhibit atherosclerosis progression. The fixed association of atorvastatin, perindopril and amlodipine under the name of Lipertance is the first fixed combination of these three groups to control the risk factors that are hypertension and dyslipidemia which can be used both in primary and secondary cardiovascular prevention .

NCT ID: NCT04307810 Not yet recruiting - Child Behavior Clinical Trials

Parent Predicting of Their Child Behavior During Their First Dental Examination

Start date: April 15, 2020
Phase:
Study type: Observational

The aim of this study is to assess the parental expectation for their child behavior in a group of children with primary dentition during their first dental examination