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NCT ID: NCT03289871 Completed - Onychomycosis Clinical Trials

Clinical Evaluation of the Efficacy of a Medical Device in Treatment of Toenail Onychomycosis

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

This study evaluates the effect of the medical device "Excilor® Fungal Nail Infection" in the treatment of toenail onychomycosis. Half of the participants will receive the tested product and the other half will receive a comparator (Amorolfin 5%). Patients will be followed during 6 months.

NCT ID: NCT03262675 Not yet recruiting - Heart Failure Clinical Trials

NAtional TUnisian REgistry of Heart Failure

NATURE-HF
Start date: October 2, 2017
Phase: N/A
Study type: Observational [Patient Registry]

NATURE-HF is an observational, multicentric and longitudinal study of heart failure performed with 100 tunisian cardiologists.

NCT ID: NCT03260439 Completed - Clinical trials for Tramadol - Anesthetics- Child - Circumcision

Tramadol in Penial Block Does it Improve Efficiency of Postoperative Analgesia in Circumcision

Start date: June 2014
Phase: N/A
Study type: Interventional

After the consent of the local ethics committee and informed consent of the parents, we conducted a prospective randomized, double-blind study, from 30 June 2014 to 31 December 2014, including one to eight year olds, ASA I or II and Programmed for circumcision.We collected 53 children in each group.

NCT ID: NCT03257800 Completed - Laryngeal Masks Clinical Trials

Laryngeal Mask Insertion Conditions And Hemodynamic Effects

Start date: June 1, 2013
Phase: N/A
Study type: Interventional

This interventional double-blind, randomized trial has included120 children of American Society of Anesthesiologist (ASA) physical status I or II aged between 1and 8 years of either sex, scheduled for outpatient minor surgery under general anesthesia.This study examined whether co-induction with ketamine-propofol enhance laryngeal mask airway (LMA) insertion conditions and preserve hemodynamic state in patients.

NCT ID: NCT03255239 Recruiting - Ventral Hernia Clinical Trials

Open Preperitoneal Mesh Versus Retromuscular Mesh Versus Suture Repair for Abdominal Wall Hernias

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

Randomized clinical trial comparing open preperitoneal mesh, retromuscular mesh and suture repair for ventral hernias less than 3 cm diameter

NCT ID: NCT03241875 Completed - Pain, Postoperative Clinical Trials

Effects of Preoperative Gabapentin Versus Pregabalin on Shoulder Pain After Laparoscopic Cholecystectomy

Start date: December 1, 2016
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the effect of premedication with pregabalin or gabapentin versus placebo on postoperative shoulder pain after laparoscopic cholecystectomy.

NCT ID: NCT03241069 Completed - Acute Heart Failure Clinical Trials

Dynamic Variation of Impedance Cardiography(DYVIC) as a Diagnostic Tool of Acute Heart Failure (AHF)

DYVIC
Start date: July 2012
Phase: N/A
Study type: Interventional

Dynamic variations of bio-impedance measured cardiac output using pharmacologic (inhaled nitrate) and non pharmacologic intervention (sitting position, passive leg rising and valsalva maneuver) could be used to detect acute heart failure in patients admitted to the ED for dyspnea.

NCT ID: NCT03240510 Active, not recruiting - Male Breast Cancer Clinical Trials

Understanding Male Breast Cancer: Salah Azaïz Cancer Institute Experience

Start date: January 1, 2014
Phase: N/A
Study type: Observational

The goal of this study is to evaluate the Salah Azaïz Cancer Institute male breast cancer patients population over a period of 14 years. Goal of the retrospective part: to gather clinicopathologic data and follow-up outcomes of male breast cancer patients diagnosed and/or treated at Salah Azaïz Cancer Institute from 2004 to 2013. Goal of the prospective part: to create a registry of male patients with breast cancer for a period of 48 months (from 2014 to 2017).

NCT ID: NCT03233035 Recruiting - Trauma Clinical Trials

Ketamine Intra Nasal Traumatology

Ket
Start date: October 1, 2016
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy and safety of early administration of low-dose intranasal ketamine analgesic agents in patients with moderate to severe pain in the ED in reducing the need for opioid or class III analgesic agents.

NCT ID: NCT03222518 Recruiting - Clinical trials for Acute Pain Due to Trauma

NSAIDs Versus Paracetamol Versus Paracetamol + NSAIDs in Traumatic Pain Management

Start date: August 1, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to: Compare the effect of paracetamol alone against NSAIDs alone against the association of paracetamol + NSAIDs in the treatment of traumatic pain.