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NCT ID: NCT03085576 Completed - Atrial Fibrillation Clinical Trials

NATional TUnisian REgistry of Atrial Fibrillation

NATURE-AF
Start date: March 1, 2017
Phase:
Study type: Observational [Patient Registry]

A non-interventional, national longitudinal study of atrial fibrillation performed with 91 cardiologists.

NCT ID: NCT03075566 Recruiting - Clinical trials for Coronary Artery Disease

Coronary Artery Disease: a Case- Control Study

Start date: September 2014
Phase: N/A
Study type: Observational

Atherosclerosis is a chronic inflammatory condition, which is associated by the involvement of several pathological events, and alteration in the serum levels of pro- and anti-inflammatory, and lipid markers. The investigators evaluated the contribution of serum biomarkers levels to the pathogenesis of coronary artery disease, namely their association with risk factors, clinical presentation, extent and severity of atherosclerotic changes accompanying coronary artery disease.

NCT ID: NCT03072329 Completed - Penile Surgery Clinical Trials

Neurostimulation in Pudendal Nerve Block

Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to check whether the success rate of blind pudendal nerve block in penile surgery can be optimized by the search for a motor response during neurostimulation.

NCT ID: NCT03017248 Active, not recruiting - Pain Clinical Trials

Low-dose Ketamine for Acute Pain in the Emergency Department

Start date: January 2016
Phase: Phase 1
Study type: Interventional

This study aims to determine the efficacy and safety of low dose ketamine in association with IV morphine in the management of acute moderate to severe pain in emergency department. The investigators hypothesize that low dose ketamine will result in more effective pain control than morphine alone and will not be associated with an increase in adverse events.

NCT ID: NCT02978690 Completed - Psoriasis Clinical Trials

Spesolimab (BI 655130) Single Dose in Generalized Pustular Psoriasis

Start date: December 19, 2016
Phase: Phase 1
Study type: Interventional

This is a phase I, open label, single group study that is being performed to assess the safety, tolerability, Pharmacokinetics (PK) , Pharmacogenomics (PGx) and efficacy of a single dose of spesolimab in adult patients with active Generalized Pustular Psoriasis (GPP).

NCT ID: NCT02963454 Recruiting - Septic Shock Clinical Trials

Effects of Levosimendan on Cellular Metabolic Alterations in Patients With Septic Shock

Start date: January 2011
Phase: N/A
Study type: Interventional

To investigate changes in the concentration of glucose, lactate, pyruvate and glycerol in the extracellular fluid of the skeletal muscle following levosimendan administration in patients with septic shock.

NCT ID: NCT02962700 Recruiting - Septic Shock Clinical Trials

Effects of Continuous Haemofiltration vs Intermittent Haemodialysis on Microcirculatory Parameters in Septic Shock

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

The aim of the study was to investigate whether CVVH, in comparison to intermittent haemodialysis (IHD), is able to improve regional perfusion in septic shock patients studied by muscle microdialysis

NCT ID: NCT02854787 Completed - Hypotension Clinical Trials

Intravenous Bolus of Phenylephrine vs. Norepinephrine in Preventing Hypotension After Spinal Anesthesia

NorPN
Start date: May 2016
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine if an intravenous bolus of phenylephrine is more effective compared to an intravenous bolus of norepinephrine associated with crystalloid loading for maintaining blood pressure during a spinal anesthetic for a cesarean delivery. Prevention of low blood pressure has been shown to decrease nausea and vomiting during and after cesarean delivery under spinal anesthesia. For elective cesarean delivery, all participants will receive spinal anesthesia with a local anesthetic and sufentanil. This study plans to enroll 120 pregnant women. Patients will be randomly assigned according to a computer generated system to be in one of two groups.

NCT ID: NCT02853058 Recruiting - Labor Complication Clinical Trials

Uterine Artery Pulsatility Index and Materno Fetal Outcomes

UADLAB
Start date: July 2016
Phase: N/A
Study type: Interventional

High Uterine artery index pulsatility (PI) is associated with small for gestationnal age but also with stillbirth and distress during labor.

NCT ID: NCT02847936 Recruiting - Episiotomy Clinical Trials

Efficacy of Triclosan-coated Sutures in the Episiotomy

EPISIOVIC
Start date: July 2016
Phase: Phase 4
Study type: Interventional

Surgical repair of perineal lesions after delivery can be associated with infection of the surgery site. The aim of this study was to compare the surgical site infection with triclosan-coated suture (Vicryl Plus) versus coated suture (Vicryl) in the episiotomy after delivery.