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NCT ID: NCT03433521 Completed - Clinical trials for Acute Myeloid Leukemia

Observational Study of Spatio-Temporal Patterns of New Cases of Acute Myeloid Leukemia

Start date: January 1, 2018
Phase:
Study type: Observational

Published data regarding the temporal pattern of AML are scarce and old. The greater knowledge of these neoplasias has made that their classification has been remarkable modified. Therefore, we consider relevant to carry out the present study as it would allow us to analyze the potential existence of a spatio-temporal pattern in the incidence of AML in Spain.

NCT ID: NCT03433482 Completed - Clinical trials for Meningitis, Meningococcal

A Study to Investigate the Safety and Immunogenicity of Different Formulations of GSK Biologicals' Meningococcal ACWY Conjugate Vaccine (GSK3536820A and Menveo) Administered to Healthy Adolescents and Young Adults 10 to 40 Years of Age

Start date: August 30, 2018
Phase: Phase 2
Study type: Interventional

MenACWY (Menveo) is a GSK vaccine intended for protection against disease caused by meningococcal bacteria groups A, C, W and Y in infants, children and adults, licensed in more than 60 countries. The purpose of this study is to compare the immunogenicity of the currently licensed MenACWY vaccine with the investigational MenACWY liquid vaccine aged for different lengths of time by storage at 2-8ºC.

NCT ID: NCT03432988 Completed - Renal Dialysis Clinical Trials

Impact of Nurses´ Solution-focused Communication on the Fluid Adherence of Adult Patients on Hemodialysis

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

Aim: To test the hypothesis that fluid adherence in patients on hemodialysis can be improved through nurses´ solution-focused communication with patients on issues of adherence. Design: Single-group quasi-experimental study. Method: A one-month baseline of inter-dialytic weight gain was taken for a group of 36 adult patients in a hospital hemodialysis unit. Then, the nurses of the unit received an 5-hour training in solution-focused communication on issues of fluid adherence and applied it with the patients of the sample. Inter-dialytic weight gains (IDWG) were measured during another month. Six months after the training, IDWG was again measured during one month.

NCT ID: NCT03432104 Completed - Clinical trials for Dietary Modification

Evaluation of Bioavailability of Phenolic Compounds From Oxxynea®

Start date: February 23, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate bioavailability and pharmacokinetics of phenolic compounds from Oxxynea®, a blend of fruit and vegetable extracts, in healthy volunteers, during a randomized, double-blind and cross-over trial. After a single dose supplementation, both metabolic profile and urinary excretion will be determined over a 48h-period by means of High-Performance Liquid Chromatography coupled with a tandem mass spectrometry (HPLC-MS) to identify and quantify phenolic metabolites. In parallel, post-prandial potential anti-oxidative and anti-glycemic properties of Oxxynea® will be determined in blood, following consumption of a cafeteria-type breakfast.

NCT ID: NCT03430843 Completed - Clinical trials for Esophageal Squamous Cell Carcinoma (ESCC)

A Study of Tislelizumab (BGB-A317) Versus Chemotherapy as Second Line Treatment in Participants With Advanced Esophageal Squamous Cell Carcinoma

Start date: January 26, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate the efficacy and safety of tislelizumab as second line treatment in participants with advanced unresectable/metastatic ESCC that had progressed during or after first line therapy.

NCT ID: NCT03430219 Completed - Bone Marrow Edema Clinical Trials

Subchondroplasty Procedure in Patients With Bone Marrow Lesions

Start date: March 1, 2018
Phase:
Study type: Observational

This is a prospective, multi-center, post-market data collection study intended to collect data on the short- and long-term safety and performance of the SCP Procedure.

NCT ID: NCT03429998 Completed - Clinical trials for Hypercholesterolemia

Evolocumab Versus LDL Apheresis in Patients With Hypercholesterolemia

Start date: April 1, 2017
Phase: Phase 3
Study type: Interventional

An open-label, prospective phase III study to compare the efficacy and safety of administering evolocumab versus treatment with LDLapheresis in patients with familial hypercholesterolemia and high cardiovascular risk.

NCT ID: NCT03429881 Completed - Endometriosis Clinical Trials

Microparticle Generation After Laparoscopic Surgical Treatment for Endometrioma.

Start date: February 5, 2018
Phase: N/A
Study type: Interventional

Study objective: To evaluate serial generation of microparticles (MPs) after laparoscopic stripping or CO2 laser vaporization in surgical treatment of patients with ovarian endometrioma (OE). Design: A prospective, randomized, blinded, pilot study, including 33 patients. Setting: Tertiary university hospital from April 2015 to June 2017. Patients: 33 women with unilateral OE undergoing laparoscopic surgery. Intervention: Patients were randomly selected to undergo either CO2 laser vaporization (L group) or laparoscopic stripping (S group) of OE. Measurements and Main results: Blood samples were collected before surgery, and at 2 hours, 24 hours, 1 month, and 3 months after surgery. MPs generation curve after ovarian endometrioma surgery was performed.

NCT ID: NCT03429452 Completed - Clinical trials for Structural Heart Abnormality

The SALMANTICOR Study

SALMANTICOR
Start date: October 15, 2015
Phase:
Study type: Observational [Patient Registry]

The SALMANTICOR study will obtain data on the prevalence and incidence of structural heart disease in a population setting. A cross-section survey of randomly selected residents of Salamanca (Spain) will be performed. A total of approximately 2400 individuals, stratifies by place of residence (rural and urban) and by age and sex will be studied. The variables to analyzed will be obtained from the clinical history, different surveys including social status, Mediterranean diet, functional capacity, electrocardiogram, echocardiogram and biochemical and genetic analysis. Surviving participants are expected to return for a 5 and 10-year follow-up visit.

NCT ID: NCT03429231 Completed - Health Status Clinical Trials

Observational Study to Evaluate the Quality of Life of Healthy Postmenopausal Women Who Take Coenzyme Q-Ubiquinol

Start date: November 23, 2017
Phase:
Study type: Observational

Observational study about quality of life in postmenopausal women taking coenzyme Q compared to another group of women of the same age who do not take it