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NCT ID: NCT04018950 Completed - Clinical trials for Acinetobacter Baumannii-calcoaceticus Complex Infections

Study to Determine the Excretion and Metabolism of 14C-ETX2514 Administered Intravenously in Healthy Male Subjects

Start date: June 21, 2019
Phase: Phase 1
Study type: Interventional

This study will be conducted to determine the routes and rates of excretion of radio label arising from 14C-ETX2514 and to characterize metabolites of ETX2514 arising from 14C-ETX2514 administered intravenously in healthy participants.

NCT ID: NCT04018794 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder Symptoms

Development of a Mobile App for an Executive Functioning Intervention for Adolescents

Start date: September 30, 2019
Phase: N/A
Study type: Interventional

This study develops an initial prototype of a mobile tool that will support clinician-directed behavioral/organizational skills treatment for adolescents with Attention Deficit Hyperactivity Disorder (ADHD) with input guided from key stakeholders.

NCT ID: NCT04018781 Completed - Clinical trials for Medication Reconciliation at Discharge

Guaranteeing the Continuity of the Care Pathway for the Elderly Patient: Evaluation of a Territorial Approach of Clinical Pharmacy

CONPARMED
Start date: June 13, 2019
Phase:
Study type: Observational

In the context of the ageing of the French population, drug iatrogeny in the elderly is a major public health issue, responsible for approximately 7,500 deaths per year and 3.4% of hospitalizations among patients aged 65 and over. The interest of the Medication Reconciliation (MR) in reducing medication errors and unintentional discrepancies in prescriptions at transition points in patients' medication care pathways no longer seems to be in doubt both in France and abroad. On the other hand, the literature on the clinical impact of these drug errors (i. e. occurrence of an adverse drug event (ADE) or readmission rates) is currently limited in France and presents variable results abroad.

NCT ID: NCT04018599 Completed - Clinical trials for Rheumatoid Arthritis

Comparison of PK and Tolerability of MSB11022 Administered by AI or PFS

Start date: July 15, 2019
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to demonstrate equivalence of the pharmacokinetic (PK) profile of MSB11022 administered by either an auto-injector (AI) or a pre-filled syringe (PFS) as single subcutaneous (s.c.) injection of 40 mg.

NCT ID: NCT04018261 Completed - CMV Viremia Clinical Trials

Virus-specific Activated T Lymphocytes From a Donor in Hematopoietic Progenitor Transplanted Patients

Start date: July 4, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Marrow transplanted immunocompromised patients with cytomegalovirus (CMV) viral infection will be treated with CMV activated T-Lymphocytes. T-Lymphocytes will be obtained through an apheresis from a compatible donor. Safety and immunoreconstitution parameters in blood samples will be assessed up to +60 days after the treatment.

NCT ID: NCT04018079 Completed - Clinical trials for Congenital Heart Disease in Children

Left Ventricular Dysfunction Post-surgical Patent Ductus Arteriosus Ligation in Children: Predictor Factors Analysis

Start date: June 1, 2015
Phase:
Study type: Observational [Patient Registry]

Background: PDA is viewed as a standout amongst the most widely recognized congenital heart defects in children and its closure is responsible for many hemodynamic changes that require intervention and care. Methods: A retrospective study included fifty children with isolated PDA treated by surgical ligation from June 2015 to June 2018. Their mean age was 15.78 ± 7.58 months and 72% were females. The LV dimensions and systolic function were assessed by two-dimensional echocardiography pre PDA ligation. The mean duct size was 4.08 ± 1.25 mm.

NCT ID: NCT04017754 Completed - Clinical trials for Pregnancy Complications

Low Plasma Mannose Binding Lectin (p-MBL) Level is a Risk Factor for Recurrent Pregnancy Loss (RPL)

Start date: January 1, 2016
Phase:
Study type: Observational

The present study is based on the hypothesis, that recurrent pregnancy loss (RPL) is associated with abnormal plasma mannose binding lectin (p-MBL) level. Secondarily, p-MBL level may affect the reproductive and the perinatal outcome in the first pregnancy following RPL. Thus, the present study aim to examine whether MBL should be a biomarker for women at risk for RPL and, secondarily, affect the reproductive and perinatal outcome, and thereby help clinicians identify fragile women who need intensified perinatal care.

NCT ID: NCT04017156 Completed - Clinical trials for Edentulous; Alveolar Process, Atrophy

Bone Healing at Non-submerged Implants Installed With Different Insertion Torques.

Start date: July 20, 2016
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate histomorphometrically the healing at implants installed with standard or very low insertion torque values.

NCT ID: NCT04017000 Completed - Clinical trials for Diagnosis of Urinary Tract Symptons

Bladder Shaper Test

BlaST
Start date: April 2, 2019
Phase: N/A
Study type: Interventional

This study is comparing a novel method of Bladder shape measurements using ultrasound for diagnosis of lower urinary tract symptoms in comparison to traditional Urodynamic assessment. All participants will undergo the novel investigation followed by their usual Urodynamics.

NCT ID: NCT04016779 Completed - Clinical trials for Attention-Deficit/Hyperactivity Disorder (ADHD)

Evaluation of SPN-812 (Viloxazine Extended-release Capsule) in Adults With ADHD

Start date: November 20, 2019
Phase: Phase 3
Study type: Interventional

This study will evaluate the efficacy and safety of SPN-812 (Viloxazine extended-release capsules; 200-600 mg) in adults 18-65 years of age with Attention-Deficit/Hyperactivity Disorder (ADHD).