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NCT ID: NCT04021251 Recruiting - Diabetes Clinical Trials

Performance Characteristics of Non-invasive Glucose Monitoring Device Prototypes

Start date: December 20, 2018
Phase: N/A
Study type: Interventional

This clinical study has been launched to collect spectral raman data paired with validated glucose reference values in private homes of subjects

NCT ID: NCT04021186 Recruiting - Clinical trials for Surgery--Complications

An Optimization in the Postoperative Treatment in Head and Neck--surgical Patients.

Start date: July 5, 2019
Phase: N/A
Study type: Interventional

Based on glycemic load (overall increase in blood glucose), it is investigated whether better glycemic control (large fluctuations in blood glucose to abnormal values are attempted) can improve the postoperative phase of head and neck surgical patients who receive Dexamethasone (glucocorticoid). Furthermore it is examined whether this optimization in treatment can result in reduced hospitalization time and fewer re-admissions. Hypothesis: Continuous blood glucose measurement and insulin therapy will optimize the postoperative phase of the embedded head and neck patient receiving Dexamethasone by reducing the incidence of hyperglycaemia and associated complications.

NCT ID: NCT04015141 Recruiting - Clinical trials for Partial-onset Seizures

A Study to Evaluate Efficacy and Safety of Perampanel Administered as an Adjunctive Therapy in Pediatric Participants With Childhood Epilepsy

Start date: May 31, 2019
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the efficacy of perampanel as measured by the 50 percent (%) responder rate during the maintenance period of the core study for seizure frequency in participants with pediatric epileptic syndrome (Cohort 1) and partial-onset seizures (POS) (Cohort 2).

NCT ID: NCT04012788 Recruiting - Clinical trials for Clostridium Difficile Infection

CDI Synbiotic Study

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

The investigators hypothesize that treatment with a synbiotic mixture consisting of inulin Lactobacillus rhamnosus (LGG®), Lactobacillus acidophilus (LA-5®), Lactobacillus paracasei (L. casei 431®) and Bifidobacterium lactis (BB-12®) can reduce the number of C. difficile recurrences significantly.

NCT ID: NCT04008030 Recruiting - Clinical trials for Metastatic Colorectal Cancer

A Study of Nivolumab, Nivolumab Plus Ipilimumab, or Investigator's Choice Chemotherapy for the Treatment of Participants With Deficient Mismatch Repair (dMMR)/Microsatellite Instability High (MSI-H) Metastatic Colorectal Cancer (mCRC)

CheckMate 8HW
Start date: August 5, 2019
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to compare the clinical benefit, as measured by Progression-Free Survival (PFS), Objective Response Rate (ORR), and Overall Survival (OS), achieved by nivolumab in combination with ipilimumab or by nivolumab monotherapy in participants with Microsatellite Instability High (MSI-H) or Mismatch Repair Deficient (dMMR) metastatic colorectal cancer (mCRC). This study will also compare nivolumab plus ipilimumab combination vs chemotherapy for treatment of MSI-H/dMMR mCRC participants.

NCT ID: NCT04006405 Recruiting - Clinical trials for Clear Cell Renal Cell Carcinoma

AURORAX-0087A: GAG Scores for Surveillance of Recurrence in Leibovich Points ≥5 Non-metastatic ccRCC

AUR87A
Start date: January 10, 2020
Phase:
Study type: Observational

AUR87A is an observational prospective multicenter diagnostics test cohort study for detection of renal cell carcinoma recurrence as determined by the reference standard, which is imaging using computed tomography (CT) of the chest and abdomen at defined intervals after primary surgery.

NCT ID: NCT03999723 Recruiting - Clinical trials for Acute Myeloid Leukemia

Combining Active and Passive DNA Hypomethylation

EVI-3
Start date: September 11, 2019
Phase: Phase 2
Study type: Interventional

This is a multicentre, randomized, parallel-group, placebo-controlled, double-blind phase 2 study of the efficacy and safety of oral vitamin C supplement in combination with azacitidine in patients with higher-risk MDS, CMML-2 or low-blast count AML. The primary purpose is to investigate if oral vitamin C supplementation to azacitidine, compared with azacitidine + placebo, can increase the effectiveness of epigenetic therapy in patients with higher-risk myeloid malignancies, who are not candidates for allogeneic hematopoietic stem cell transplantation.

NCT ID: NCT03994471 Recruiting - Clinical trials for End Stage Renal Disease

Efficacy and Safety of XyloCore Peritoneal Dialysis Solution.

ELIXIR
Start date: December 14, 2022
Phase: Phase 3
Study type: Interventional

Randomized, controlled, parallel groups, open-label, blinded end-point assessment, multicenter study, comparing the effects of a low glucose peritoneal dialysis solution, XyloCore, to glucose solutions (Physioneal, Fixioneal, Dianeal, Balance, Bicavera, Bicanova or Equibalance) only regimen, in patients with End-Stage Renal Disease (ESRD) receiving Continuous Ambulatory Peritoneal Dialysis (CAPD), over a 6-month study period.

NCT ID: NCT03986827 Recruiting - Clinical trials for Social Anxiety Disorder

Cognitive Behavioral Therapy for Adolescents With Social Anxiety Disorder

Start date: February 28, 2019
Phase: N/A
Study type: Interventional

The main aim of the present study is to investigate the effectiveness of a disorder specific group cognitive behavior therapy (G-CBT) program for youth SAD, the, Cool Kids Anxiety Program - Social Enhanced (CK-E), developed at Macquarie University, Sidney, Australia. Furthermore, the study will examine how well this program fares against generic CBT treatment.

NCT ID: NCT03981510 Recruiting - Constipation Clinical Trials

Comparison of Gastrointestinal Motility in Healthy Children and Children With Constipation

Start date: June 13, 2019
Phase: N/A
Study type: Interventional

To gain a better understanding of the underlying dysmotility in constipation in children, we will use a novel minimal invasive method called 3D Transit. We will examine four groups of children aged 7 to 17 years: healthy children, chronically constipated children (ROM IV criteria), children with neurofibromatosis type 1 and finally children receiving chemotherapy (vincristin) for acute lymphoblastic leukemia.