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NCT ID: NCT03480269 Not yet recruiting - Clinical trials for Predictors of Response to HCV Tretment

Very Rapid and Rapid Virological Response as Predictors of Response of HCV Tretment

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

assessment of very rapid virological response and rapid virological response as predictors of response to sofosbuvir and daclatasvir in treatment of cirrhotic and non-cirrhotic patients with HCV, eligible to treatment.

NCT ID: NCT03476031 Not yet recruiting - Clinical trials for Cryoglobulinaemia Due to Chronic Hepatitis C

Pathology of Hepatitis c Nephropathy

Start date: November 2018
Phase:
Study type: Observational

Hepatitis c associated glomerulonephritis is an immune complex disease that occurs in 21% of patients who have HCV infection.

NCT ID: NCT03471312 Not yet recruiting - Clinical trials for Magnesium Therapy on Cerebral Palsy Patients

Effect of Oral Magnesium Therapy on Constipation on Cerebral Palsy Children

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

The aim of this study is to study the therapeutic and adverse effects of oral magnesium sulfate therapy on constipation in children with spastic cerebral palsy suffering from chronic constipation in neuro pediatric unit at Assiut University Hospital.

NCT ID: NCT03469973 Not yet recruiting - Clinical trials for Velopharyngeal Insufficiency

Partial Adenoidectomy in Cases of Velopharyngeal Dysfunction

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

The velopharyngeal valve is a tridimensional muscular valve that is located between the oral and nasal cavities. It consists of the lateral and posterior pharyngeal walls as well as the soft palate. The role of the velopharyngeal valve is to separate the oral and nasal cavities during speech and swallowing.

NCT ID: NCT03468556 Not yet recruiting - Clinical trials for NASH - Nonalcoholic Steatohepatitis

A Randomized, Double-Blind, Placebo Controlled Study to Assess the Efficacy and Safety of SNP-610 for the Treatment of Patients With Non-alcoholic Steatohepatitis

Start date: March 1, 2024
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to compare the changes in serum ALT level among patients with non-alcoholic steatohepatitis (NASH) following 3-month treatment of 800 mg SNP-610 or the placebo. The secondary objectives will be to compare the changes in liver fat fraction, other liver function tests, cytokeratin-18 (CK-18) fragment level and adverse event / serious adverse event rates among the interventional and placebo arms.

NCT ID: NCT03468296 Not yet recruiting - Clinical trials for Neovascular Age-related Macular Degeneration

Two-week Retreatment Interval Study for Treated Age-related Macular Degeneration Refractory to Monthly Aflibercept

TRISTAR
Start date: April 2018
Phase: Phase 4
Study type: Interventional

This study is designed to evaluate the safety and efficacy of every 2 week intravitreal aflibercept injections in a population of neovascular AMD patients that have demonstrated refractory subretinal fluid with or without intraretinal fluid despite prior monthly intravitreal aflibercept treatment.

NCT ID: NCT03466645 Not yet recruiting - Clinical trials for Elective Craniotomy-candidated Patients

The Effectiveness of Vancomycin in Comarison With Cefazolin in Prevention of SSI After Craniotomy

Start date: April 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Surgical-site infection is the most commonly reported nosocomial infection in patients undergoing surgery and 3rd most nosocomial infection in hospitalized patients. The SSI is associated with increases of length of hospitalization for 6 days and increases the hospital's cost by $ 300. Because of these, prevention of SSI with appropriate antibiotic is essential.

NCT ID: NCT03463291 Not yet recruiting - Clinical trials for Efficacy of MRI Diffusion in Differentiation Between Benign and Malignant Bony Lesions

Role of MRI Diffusion in Differentiation Between Benign and Malignant Bony Lesions

Start date: May 2018
Phase: N/A
Study type: Observational

Bone tumors are categorized according to their tissue of origin into cartilagenous, osteogenic, fibrogenic, fibrohistiocytic, haematopoietic, vascular, and lipogenic tumors. Magnetic resonance imaging (MRI) is now indispensable for the preoperative workup and therapeutic follow-up of patients with musculoskeletal tumors. The application of DW-MRI in bone marrow is today an established examination technique that provides a unique contrast and that can help in the detection of bone-marrow pathologies and the differentiation of benign and malignant bone-marrow lesions. Diffusion MRI provides quantitative and qualitative assessments of tissue cellularity and cell-membrane integrity. It is widely used for tumour detection, characterisation, and monitoring during treatment. Diffusion MRI supplies functional information that complements the structural evaluation. In combination with standard structural MRI parameters, the ADC value improves tumour characterization. Diffusion MRI can also be used to monitor tumours during chemotherapy. Tumour necrosis results in loss of cell membrane integrity and in expansion of the extracellular compartment, leading to greater water-molecule diffusion with an increase in the ADC value.

NCT ID: NCT03462433 Not yet recruiting - Clinical trials for Unruptured Intracranial Aneurysms

Treatment of Ruptured Intracranial Aneurysms in China.

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

Ruptured intracranial aneurysms is currently a common disease that seriously affects human health and quality of life due to its high morbidity,high mortality and high disability. At present,Ruptured intracranial aneurysms are treated with craniotomy clipping and interventional embolization ,but for ruptured wide-neck intracranial aneurysms, the treatment of craniotomy clipping and coiling embolization are not effective.With the improvement of endovascular treatment materials and techniques, three dimensional coil basket technique, double microcatheter technique, balloon assisted ONYX embolization, simple stent covered aneurysm neck, balloon or stent assisted neck remodeling and coil embolization are used in endovascular treatment of ruptured wide-neck intracranial aneurysms. The treatment methods are different in the intervention effect of ruptured wide-neck intracranial aneurysms, for example, the complications of interventional therapy are lower than craniotomy clipping,but the rate of well functional outcome (mRS ≤2) differed significantly by 3 months follow-up (65.0% vs.75.0%), and there is not standard of treatment in different parts of ruptured wide-neck intracranial aneurysms in our country, the choice of interventional therapy or craniotomy clipping are different in different clinical centers; on the other hand, there are serious problems in the treatment of ruptured wide-neck intracranial aneurysms, because without the relevant guidelines of diagnosis and treatment of ruptured wide-neck intracranial aneurysms, different clinical centers will cause excessive treatment of ruptured wide-neck intracranial aneurysms, not only bring unreasonable utilization of medical resources, but also cause the subject's life and property to be threatened. The patients with ruptured wide-neck intracranial aneurysms(n=1084) and unruptured intracranial aneurysms(n=300) were included in prospective cohort study, after interventional therapy and craniotomy clipping, setting fixed time for postoperative follow-up, the clinical data and image data were recorded, the safety, efficacy and economic benefits of interventional treatment and craniotomy clipping were compared, providing strategies for the standardized treatment of ruptured wide-neck intracranial aneurysms.

NCT ID: NCT03462160 Not yet recruiting - Clinical trials for Prevention of Urinary Tract Infections in Children

Effectiveness of Probiotics Prophylaxis of Urinary Tract Infections in Children

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The investigators aim to assess the effectiveness of prophylaxis of urinary tract infections in children with a probiotic containing Lactobacillus rhamnosus PL1 and Lactobacillus plantarum PM1. It is formulated a hypothesis that a 3-months course of probiotic prophylasis is more effective than placebo.