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NCT ID: NCT03589495 Completed - Clinical trials for Systemic Inflammatory Response Syndrome

Safety and Efficacy of Adding Intravenous N-acetyl Cysteine in Colon Surgeries

Start date: July 30, 2015
Phase: Phase 4
Study type: Interventional

The use of antioxidant agents in the prevention or decreasing the severity of postoperative systemic inflammatory response syndrome after colonic surgeries adopted nowadays. Therefore, it is of interest to investigate safety and efficacy of administrating short term intravenous (IV) N acetyl cysteine as add on to l alany l glutamine and total parenteral nutrition on the marker of oxidative stress malondialdehyde and anti- inflammatory marker tumor necrosis factor alpha in patients undergoing colonic surgeries through a prospective, randomized, double blinded, controlled clinical trial

NCT ID: NCT03589482 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Assessing Lung Inhomogeneity During Ventilation for Acute Hypoxemic Respiratory Failure

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

Mechanical ventilation can cause damage by overstretching the lungs, especially when the lungs are collapsed or edematous. Raising ventilator pressures can reduce lung collapse and this can prevent overstretching from mechanical ventilation. It remains uncertain how much pressure (PEEP - positive end-expiratory pressure) should be used on the ventilator and how to identify patients who will benefit from higher ventilator pressures vs. lower ventilator pressures. The investigators are using a unique new imaging technology, electrical impedance tomography (EIT), to study this problem and to determine the safest and most effective ventilator pressure level. The results of this study will inform future trials of higher vs. lower PEEP strategies in mechanically ventilated patients.

NCT ID: NCT03589469 Completed - Clinical trials for Diffuse Large B-cell Lymphoma Recurrent

Study to Evaluate the Efficacy and Safety of Loncastuximab Tesirine in Patients With Relapsed or Refractory Diffuse Large B-Cell Lymphoma

LOTIS-2
Start date: August 1, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this Phase 2 study is to evaluate the clinical efficacy and safety of Loncastuximab Tesirine (ADCT-402) in patients with relapsed or refractory Diffuse Large B-Cell Lymphoma.

NCT ID: NCT03589391 Completed - Clinical trials for Non Invasive Monitoring of Loss of Resistance During Epidural Injection

New Mechatronic Device for Epidural Space Detection

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

This study sought to perform the feasibility assessment of a new, non-invasive device for Loss of Resistance (LOR) detection in clinical settings. The device in charge is a mechatronic device optimized in its configurations in order to detect Loss of Resistance while performing epidural injections.

NCT ID: NCT03589300 Completed - Clinical trials for Rheumatoid Arthritis

Persona TM Tibia Clinical Outcomes Study

Start date: April 30, 2018
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate clinical performance for the commercially available Persona TM Tibia used in primary cementless tibia total knee arthroplasty.

NCT ID: NCT03588884 Completed - Clinical trials for Vitamin D Insufficiency

Repeated-dose Safety, Efficacy, Pharmacokinetic and Pharmacodynamic of CTAP101, Immediate-release Calcifediol, High-dose Cholecalciferol, and Paricalcitol Plus Low-dose Cholecalciferol in Patients With Secondary Hyperparathyroidism, Chronic Kidney Disease 3-4 and Vitamin D Insufficiency

Start date: June 8, 2018
Phase: Phase 4
Study type: Interventional

An Open-Label, Repeated-Dose Safety, Efficacy, Pharmacokinetic and Pharmacodynamic Study of Oral CTAP101 Capsules, Immediate- Release (IR) Calcifediol, High-Dose Cholecalciferol, and Paricalcitol Plus Low-Dose Cholecalciferol in Patients with Secondary Hyperparathyroidism, Stage 3 or 4 Chronic Kidney Disease and Vitamin D Insufficiency

NCT ID: NCT03588338 Completed - Clinical trials for Postoperative Nausea and Vomiting

Paracetamol on Postoperative Nausea and Vomiting

Start date: July 20, 2018
Phase: Phase 4
Study type: Interventional

The drugs with both high potency and low side effects are preferred in the prevention of postoperative nausea and vomiting (PONV) which is a common problem. This prospective randomized study aimed to compare the efficacy of paracetamol on PONV in adults undergoing maxillofacial surgery.

NCT ID: NCT03588026 Completed - Clinical trials for Paroxysmal Nocturnal Hemoglobinuria (PNH)

Treating Paroxysmal Nocturnal Haemoglobinuria Patients With rVA576

CAPSTONE
Start date: June 7, 2018
Phase: Phase 3
Study type: Interventional

rVA576 for patients with Paroxysmal Nocturnal Hemoglobinuria (PNH).

NCT ID: NCT03587506 Completed - Clinical trials for Epilepsy Generalized Idiopathic Not Intractable

Periodic Limb Movement and Genetic Generalized Epilepsy

Epilepsy
Start date: September 3, 2015
Phase:
Study type: Observational

The study aimed to study the correlation between periodic limb movement occurring during sleep and the different parameters of genetic generalized epilepsy

NCT ID: NCT03587324 Completed - Clinical trials for Vascular Surgery Patient With PAD / Carotid Stenosis

Perioperative Aspirin Response in Patients Undergoing Vascular Surgery

Start date: February 2013
Phase: N/A
Study type: Interventional

Reduced antiplatelet activity (low response (LR)/high on-treatment platelet reactivity (HPR)) of aspirin (ALR) or clopidogrel (CLR) is associated with an increased risk of thromboembolic events. The prevalence figures for low-responders reported in the literature vary widely and there have been few investigations in vascular surgery patients to date. The aim of this prospective monocentric study was to increase the evidence base on vascular surgery patients and to detect any changes in the response following vascular surgery procedures.