Clinical Trials Logo

Filter by:
NCT ID: NCT02630979 Recruiting - Clinical trials for Physician Satisfaction With the Outcomes of Cytotoxic Drugs

Oncologists Satisfaction With Outcomes of Some Cytotoxic Agents

Start date: November 2015
Phase: N/A
Study type: Observational

The study measures the degree of oncology physician satisfaction with the outcomes of some cytotoxic agents.

NCT ID: NCT02622152 Recruiting - Clinical trials for Heart Defects, Congenital

Right Lateral Positioning of Postoperative Pediatric Cardiac Surgery

Start date: January 30, 2016
Phase: N/A
Study type: Interventional

Directly following cardiac surgery for congenital heart disease; patients are not receiving routine turning every two hours to prevent pressure ulcers, because a negative influence on hemodynamic parameters is assumed. Investigators have suggested that lateral position may have clinically significant effects on oxygenation in cardiac surgery patients.

NCT ID: NCT02621372 Recruiting - Portal Hypertension Clinical Trials

Correlation of Platelets Count With Endoscopic Findings in a Cohort of Egyptian Patients With Liver Cirrhosis

Start date: January 2015
Phase: N/A
Study type: Observational

Portal hypertension is a common complication of liver cirrhosis that can lead to development of esophageal varices (EV). They are abnormally dilated veins within the wall of the esophagus that lead to haemorrhage (1). Majority of patients with cirrhosis will develop EV at some point, and about third of these patients will have at least one bleeding episode because of rupture of a varix . For this reason, screening endoscopy for detection of the presence of EV should be part of the diagnostic work-up in patients with cirrhosis. This is a very important preventive step for identification of those patients with variceal bleeding risk and furthermore, identification of patients in urgent need for prophylactic treatment. All guidelines stress on screening endoscopy for early detection of EV in cirrhotic patients with portal hypertension. However this approach is limited by its invasiveness and cost effectiveness issues of screening endoscopy .

NCT ID: NCT02621359 Recruiting - Dyspepsia Clinical Trials

A Two Week Nitazoxanidebased Quadruple Regimen

Start date: January 2015
Phase: Phase 3
Study type: Interventional

Helicobacter pylori (H. pylori) infection is a global health problem as it is associated with peptic ulcers, chronic gastritis, duodenitis, and stomach cancer. Therefore, the eradication of the pathogen is of critical importance to reduce H. pylori-related complications . However, due to increasing antibiotic resistance, eradication of Helicobacter pylori has become more challenging. With a great decline in the eradication rate of standard triple therapy for Helicobacter pylori to below 70% in many countries. Treatment with triple therapy, which is the most frequently recommended, fails to eradicate H. pylori in approximately 20% of cases .

NCT ID: NCT02620605 Recruiting - Clinical trials for Ovarian Hyperstimulation Syndrome

The Influence of Timing of Cabergoline Initiation on Prevention of OHSS

OHSS
Start date: December 20, 2017
Phase: Phase 3
Study type: Interventional

Study the effect of early cabergoline administration in prevention of occurrence or decreasing the severity of OHSS in patients undergoing intra cytoplasmic sperm injection.And its effect on oocyte maturation,fertilization and pregnancy rate..

NCT ID: NCT02616731 Recruiting - Menorrhagia Clinical Trials

Oral Tranexamic Acid Versus Diosmin for Treatment of Menorrhagia in Women Using Copper IUD

Start date: September 2015
Phase: Phase 1/Phase 2
Study type: Interventional

To compare the efficacy of tranexamic acid and diosmin in reducing menstrual blood loss in women having Intra Uterine Contraceptive Device (IUD) and suffer from menorrhagia.

NCT ID: NCT02606539 Recruiting - Clinical trials for Gestational Trophoblastic Neoplasms

Surgery Plus Single Agent Chemotherapy Versus Primary Chemotherapy for Gestational Trophoblastic Neoplasms

SVCGTN
Start date: September 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Gestational trophoblastic neoplasm affect women and is sensitive to chemotherapy especially methotrexate and the investigators try to find a role of surgery plus methotrexate instead of multiple doses and cycles of chemotherapy.

NCT ID: NCT02604394 Recruiting - STEMI Clinical Trials

Rheolytic Thrombectomy in Patients With Acute STEMI and Large Thrombus Burden

Rheo-STEMI
Start date: November 2015
Phase: N/A
Study type: Interventional

Coronary obstruction by an occlusive thrombus complicating a ruptured or eroded atherosclerotic plaque is the most frequent pathologic substrate of acute myocardial infarction (AMI). Timely restoration of perfusion and thereby myocardial salvage is the single most important objective in the management of patients with ST segment-elevation myocardial infarction (STEMI). To address these uncertainties, our study aims to evaluate the role of RT in patients who are most likely to benefit from it (thrombus grade 4 and 5) using a sensitive, quantitative, and reproducible parameter; CMR-derived myocardial salvage. also, to determine whether Rheolytic Thrombectomy (RT) before conventional PCI to the culprit vessel as compared to conventional PCI (with or without MTA) results in improved myocardial salvage; and to identify clinical and angiographic determinants of any difference observed between both treatment groups.

NCT ID: NCT02594631 Recruiting - Urinary Calculi Clinical Trials

Shock Wave Lithotripsy Versus Visual Cystolitholapaxy in The Management of Patients Presenting With Calcular Acute Urinary Retention: A Randomized Controlled Trial.

Start date: March 2015
Phase: Phase 4
Study type: Interventional

The aim of the study is to compare the safety and efficacy of ESWL and visual cystolitholapaxy in management of calcular acute urine retention.

NCT ID: NCT02590484 Recruiting - Placenta Previa Clinical Trials

The Cervix as a Natural Tamponade in Postpartum Hemorrhage Caused by Placenta Previa and Placenta Previa Accreta

Start date: June 2012
Phase: N/A
Study type: Interventional

Placenta previa and placenta accrete carry significant maternal and fetal morbidity and mortality. Several techniques have been described in the literature for controlling massive bleeding associated with placenta previa cesarean sections. The aim of this study is to evaluate the efficacy and safety of the use of the cervix as a natural tamponade in controlling postpartum hemorrhage caused by placenta previa and placenta previa accreta.