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NCT ID: NCT03824717 Not yet recruiting - Clinical trials for Infraclavicular Brachial Plexus Block

MEV 90 of 0.5% Ropivacaine In Infraclavicular Blocks

MEV90ROPI
Start date: January 2019
Phase: N/A
Study type: Interventional

Nerve blocks are routinely performed perioperatively to provide anesthesia and analgesia for various surgical procedures on the upper limb. These blocks are performed with the aid of an ultrasound machine to improve the success rate. Below the clavicle approach to these nerves is used for surgeries below the elbow, forearm and hand efficiently. Ultrasound guidance for such blocks allows direct visualisation of the needle and the spread of the freezing medication (local anesthetic) in real-time therefore reducing complications and improving success rates of blocks. It may be possible that a smaller volume of local anesthetic in this setting may allow effective anesthesia while lowering the adverse effects. The aim of this study is to find out the lowest volume of the local anesthetic that will be effective in blocking the nerves adequately.

NCT ID: NCT03821571 Not yet recruiting - Clinical trials for Evaluation of Cerebral Small Vessel Disease in Patient With Primary Aldosteronism

Evaluation of Cerebral Small Vessel Disease in Patient With Primary Aldosteronism

Start date: January 25, 2019
Phase: Phase 1
Study type: Interventional

Hypertension is known to be the major risk factor for stroke. The most common cause of secondary hypertension, primary aldosteronism (PA), is characterized by the excessive secretion of aldosterone and is related to hypertension and hypokalemia. PA accounts for 3-10 % of hypertensive patients, and a higher incidence of vascular complications compared to patients with essential hypertension was observed in several studies. The vascular injury from excessive aldosterone can occur via oxidative stress and collagen remodeling, causing endothelial dysfunction and fibrosis in the vasculature. The association between cerebral small vessel disease (cSVD) and hypertension has been well studies in the past decades. However, not much study has focused on the cSVD burden in patient with PA. The goal of this study is to understand the features of cSVD in patients with PA and for the purpose of understanding the underlying pathophysiology of cerebrovascular injury in this particular patient group.

NCT ID: NCT03820869 Not yet recruiting - Clinical trials for Autism Spectrum Disorder

The Effect Of Occupational Therapy On Sensory-Based Feeding Problems

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

Feeding problems are common in individuals with Autism Spectrum Disorder (ASD).This study was planned to investigate the effect of occupational theraphy on sensory feeding problems in ASD.

NCT ID: NCT03820622 Not yet recruiting - Clinical trials for Percutaneous Coronary Intervention

The Safety and Efficacy of DIOR Balloon in Coronary Bifurcation Lesions

BEYOND-II
Start date: March 2019
Phase: N/A
Study type: Interventional

To evaluate the safety and effectiveness of paclitaxel-eluting coronary artery balloon dilation catheter (DIOR) in revascularization of coronary bifurcation lesions compared with paclitaxel-eluting balloon (Bingo), and to provide the clinical data for the formal application in China and for the approvement of China marketing.

NCT ID: NCT03817658 Not yet recruiting - Clinical trials for Esophageal Squamous Cell Carcinoma

A Phase II Study of SHR-1210 vs Placebo as Consolidation Chemotherapy After Radical Concurrent Chemoradiotherapy in Locally Advanced ESCC

Start date: October 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to observe and evaluate the efficacy and safety of SHR-1210 vs placebo as consolidation chemotherapy after radical concurrent chemoradiotherapy for unresectable locally advanced ESCC.

NCT ID: NCT03816319 Not yet recruiting - Clinical trials for Myelodysplastic Syndrome

TAK-243 in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia or Refractory Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia

Start date: August 30, 2024
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of TAK-243 in treating patients with acute myeloid leukemia, or myelodysplastic syndrome, or chronic myelomonocytic leukemia that has come back or that is not responding to treatment. TAK-243 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT03815461 Not yet recruiting - Clinical trials for Locally Advanced Pancreatic Cancer

Nab-paclitaxel Combined With S-1 as Induction Therapy for Locally Advanced Pancreatic Cancer

Start date: February 1, 2019
Phase: Phase 2
Study type: Interventional

This single-arm, Phase II clinical trial is to evaluate the efficacy and safety of nab-paclitaxel plus S-1 in locally advanced pancreatic cancer who were borderline resectable or unresectable .

NCT ID: NCT03813043 Not yet recruiting - Clinical trials for Gastro-Esophageal Reflux Disease With Ulceration

The 90% Effective Sedation Dose Of Midazolam

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

There are no clear conclusive clinical reports defining the adequate effective dose of midazolam in patients undergoing day-case esophageal-gastro-duodenoscopy (EGD). Defining such dosage will facilitate practitioners who are not anesthesia professionals to administer sedative drugs to establish a satisfactory level of moderate sedation. Our first aim is to determine the effective dose for 90% of patients (ED 90) of midazolam undergoing day-case EGD.

NCT ID: NCT03812913 Not yet recruiting - Pediatrics Clinical Trials

Neuropsychological Assessment of Children and Adolescents With Turner Syndrome

ENEAST
Start date: February 2019
Phase:
Study type: Observational

Turner syndrome (TS) is a rare chromosomal disorder characterized by partial or complete loss of one of the X chromosomes that affects about one in every 2000 female babies born. These young patients described difficulties making friends, understanding others' emotions and intentions, and controlling their own emotions. Difficulties in these domains could led to social withdrawal, to reduced social skills and could have a significant impact on self esteem and mental health as well as on long-term academic and social functioning in affected individuals. The purpose of this project is to identify functional and dysfunctional cognitive and socio-cognitive abilities in these young patients which could account social difficulties described by some of them and their family. To this end, 35 girls with TS and 35 girls with isolated growth hormone deficiency and normal cerebral MRI will be recruited. Subjects will be 7 to 16 years and 11 months of age. Socio-cognitive and cognitive functions will be assessed with neuropsychological and experimental tasks. Questionnaires completed by patient, parents or teacher, will evaluate social and behavioral functioning.

NCT ID: NCT03809754 Not yet recruiting - Clinical trials for Percutaneous Coronary Intervention

Optical Coherence Tomography Guided Percutaneous Coronary Intervention for Drug-eluting In-stent Restenosis

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

This study is a prospective, registry trial aimed to compare the clinical and angiographic outcomes of OCT-guided and angiography-guided PCI in patients with coronary DES-ISR.