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NCT ID: NCT03822091 Completed - Clinical trials for Type 1 HEPATO RENAL SYNDROME(HRS)

Terlipressin Infusion Alone Vs Terlipressin With Noradrenaline Infusion In The Treatment of Hepatorenal Syndrome Type 1

Start date: January 28, 2019
Phase: Phase 3
Study type: Interventional

Hepatorenal syndrome (HRS) is defined as a functional renal failure in a patient with chronic liver disease, or liver cirrhosis.The splanchnic circulation undergoes severe vasodilation, as a result of portal hypertension, causing an underfilling of systemic arteries.This results in intense renal vasoconstriction and functional renal failure. The best treatment options for HRS I would be a drug which has renal vasodilator property and additional splanchnic vasoconstriction. An increase in circulating blood volume would be of additional benefit. Currently Terlipressin is considered superior to other drugs in the management of HRS I. Other drugs in use are Noradrenaline and Midodrine. Albumin is added to these drugs in order to expand plasma volume. Terlipressin, a Vasopressin analog, has agonistic activity at V1 receptors. Noradrenaline acts as an agonist at α-adrenergic receptors with mild β-agonistic activity. The two major drugs used in the management of HRS act at different receptors and have completely varied mechanisms of action. Thus, a combination therapy would improve the rate of response considerably. There have been multiple studies, measuring the efficacy, safety and dosing of both drugs, but none combining both Terlipressin and Noradrenaline. Hence our study would be a pioneer in formulating a new and possibly more efficacious treatment protocol for patients of Type I HRS, in whom the treatment options are otherwise very limited. If successful, this would open new horizons of therapy for Terlipressin refractory HRS, which, otherwise is an ominous condition.

NCT ID: NCT03822052 Completed - Clinical trials for Induction of Labor Affected Fetus / Newborn

The Use of D5LR Versus LR for Induction of Labor and Time to Delivery in Multiparous and Primiparous Patient's With Favorable and Unfavorable Bishop's Scores

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

Currently, the optimum IV fluid for induction of labor is unknown. The goal of this study is to determine the optimum fluid for induction of labor, D5LR versus LR. The investigators hypothesize that patients assigned to the D5LR group will have a shorter induction of labor when compared to patient's in the LR group.

NCT ID: NCT03821727 Completed - Clinical trials for Philadelphia Positive Acute Lymphoblastic Leukemia

SCT in Ph Positive Acute Lymphoblastic Leukemia

Start date: October 26, 2016
Phase:
Study type: Observational [Patient Registry]

This study includes a registry-based, nationwide analysis to describe the clinical outcome of adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) who underwent an allogeneic hematopoietic stem cell transplantation (HSCT) after a Tyrosine Kinase Inhibitors (TKI)-based treatment.

NCT ID: NCT03821311 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Investigating the Effect of Nasal High Flow Oxygen Therapy on Regional Lung Function

INVENT
Start date: December 6, 2018
Phase: N/A
Study type: Interventional

This study aims to assess the effect of nasal high flow oxygen therapy on regional function measured by volumetric computed tomography, in patients with chronic obstructive pulmonary disease.

NCT ID: NCT03820908 Completed - Clinical trials for Acute Myelogenous Leukemia

Bisantrene for Relapsed /Refractory AML

Start date: July 18, 2019
Phase: Phase 2
Study type: Interventional

Induction of response in patients with AML that are either primary resistant (failed induction and or salvage therapy) or relapsed including post allogeneic stem cell transplantation and failed salvage therapy or cannot receive additional anthracycline .

NCT ID: NCT03820713 Completed - Clinical trials for Reduction of Postoperative Adhesions

Evaluation of the Feasibility, Safety, Initial Efficacy and Clinical Usability of FuseX Anti-Adhesion System

Start date: May 9, 2018
Phase: N/A
Study type: Interventional

Evaluation of the feasibility, safety, initial efficacy and usability of FuseX Anti-Adhesion system toward further studies that will be powered to proved its safety and efficacy. In addition, this initial study will serve to yield blood bank and surgeon feedback towards improving the system.

NCT ID: NCT03820076 Completed - Clinical trials for Study of Three Doses of AZT-04 for Skin Appearance

Safety Study of AZT-04 for Cosmetic Use

Start date: January 17, 2019
Phase: N/A
Study type: Interventional

Double Blind, Three Cohort, Placebo-controlled Trial to Assess Safety, Tolerance and Induced Bacterial Colony Counts of Three Ascending Doses of AZT-04 in Healthy Adult Volunteers

NCT ID: NCT03819634 Completed - Clinical trials for Insulin Dependent Diabetes Mellitus 1

Longevity of Multi-Slitted Catheter With Lantern Technology

Lantern
Start date: January 25, 2019
Phase: N/A
Study type: Interventional

To determine time to set failure when the Convatec Inset II with Lantern technology (Convatec Lantern) infusion set with multi-slitted catheter is worn for up to 10 days

NCT ID: NCT03819413 Completed - Clinical trials for Neuromyelitis Optica Spectrum Disorder

Clinical Patterns of Neuromyelitis Optica Spectrum Disorders in Assiut University Hospital

Start date: February 15, 2019
Phase:
Study type: Observational

Neuromyelitis Optica Spectrum Disorders (NMOSD) are a group of inflammatory demyelinating disorders of the central nervous system. Although NMOSD occurs much more commonly in nations with a predominately non-Caucasian population, NMOSD are underestimated in Egypt and frequently misdiagnosed as multiple sclerosis (MS). In this study, by investigating serum anti-aquaporin (AQP) 4 and anti-MOG antibody of patients suspected to have NMOSD attending the Neurology and Psychiatry department of Assiut University Hospital, investigators aim to determine the relative frequency, clinical and radiological characteristics of NMOSD in upper Egypt community and compare it with other populations of different races.

NCT ID: NCT03819088 Completed - Gastric Carcinoma Clinical Trials

Effects on Quality of Life With Zinc Supplementation in Patients With Gastrointestinal Cancer

Start date: April 17, 2019
Phase: N/A
Study type: Interventional

This randomized study examines how well zinc works in improving quality of life in patients with gastrointestinal cancer that cannot be removed by surgery who are receiving chemotherapy. Zinc may help to improve patient's quality of life by preventing zinc deficiency.