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NCT ID: NCT03922451 Terminated - Drug Effect Clinical Trials

Pharmacokinetics of Antibiotics During Extracorporeal Membrane Oxygenation (ECMO) Support

Start date: August 27, 2019
Phase:
Study type: Observational

This study will measure plasma concentrations of piperacillin-tazobactam and cefazolin in pediatric patients supported with extracorporeal membrane oxygenation (ECMO) aiming to better understand the pharmacokinetics of these medications in this in vivo setting.

NCT ID: NCT03830814 Completed - Drug Effect Clinical Trials

The Effects of Sacubitril/Valsartan on the Heart Functions

Start date: January 1, 2017
Phase:
Study type: Observational [Patient Registry]

Background: Sacubitril/valsartan, has been found to be more beneficial than enalapril for reducing the incidences of sudden cardiac death, death from worsening heart failure (HF), and hospitalization. However, there is no prospective echocardiographic data describing the effects of sacubitril/valsartan on the heart functions and left ventricular (LV) reverse remodeling. Therefore, the aim of our study was to evaluate the effects of sacubitril/valsartan on the LV functions using two dimensional (2D), three dimensional (3D) echocardiography and the 3D strain parameters. Methods: In 100 patients with HF with reduced ejection fraction (HRrEF) who have indications for the use of sacubitril/valsartan as recommended by recent guidelines were prospectively enrolled. The basal 2D and 3D echocardiographic parameters were compared to those obtained 3 months after starting the sacubitril/valsartan treatment.

NCT ID: NCT03801629 Completed - Drug Effect Clinical Trials

Neuroimmune Effects of Opioid Administration

NOA
Start date: September 12, 2019
Phase: Phase 1
Study type: Interventional

Preclinical research indicates acute opioid administration evokes an immune response in the periphery and brain. Here, we will translate those preclinical findings to healthy human volunteers and quantify the neuroimmune response to a morphine challenge using positron emission tomography (PET) imaging with [11C]PBR28.

NCT ID: NCT03787550 Recruiting - Drug Effect Clinical Trials

PK/PD of the Sedatives, Analgesics and Antibiotics in Patients Receiving ECMO

Start date: February 7, 2020
Phase:
Study type: Observational

It is a multi-center, open-label, observational study aimed to understand the pharmacokinetics and pharmacodynamics of the commonly used sedative, analgesic and antibiotic drugs in adult patients supported with extracorporeal membrane oxygenation (ECMO), by measuring the plasma concentrations and the clinical effect of dexmedetomidine, midazolam, butorphanol, remifentanil, sufentanil, propofol, linezolid, tigecycline, teicoplanin, caspofungin, voriconazole and meropenem.

NCT ID: NCT03745417 Not yet recruiting - Psoriasis Clinical Trials

Efficacy and Safety of Expanded UCMSCs On Patients With Moderate to Severe Psoriasis

UCMSCs
Start date: August 31, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Expanded Umbilical Cord Mesenchymal Stem Cells on patients with moderate to severe psoriasis. Any adverse events related to UCMSCs infusion will be monitored.The primary outcome is the improvement rate of PASI(Psoriasis Area and Severity Index) and treatment response will be computed from PASI before and after UCMSCs infusion.

NCT ID: NCT03635684 Completed - Pain Clinical Trials

Evaluation of Efficacy and Safety of Subcutaneous Acetaminophen

APAPSubQ
Start date: May 17, 2018
Phase: Phase 2
Study type: Interventional

Subcutaneous perfusion is an underused technique, the effectiveness of which has been demonstrated. A number of drugs of different therapeutic classes, including morphine, have a good level of scientific evidence for use by this route. Subcutaneous Acetaminophen injection is being used in some medical centers, mainly in Europe, despite the lack of definite evidence on its efficacy. This study aims to quantify the degree of effectiveness of subcutaneous Acetaminophen infusions for pain or fever in Geriatrics and Palliative Care, as well as determining its safety.

NCT ID: NCT03615820 Completed - Drug Effect Clinical Trials

Niosomal Propolis as Oromucoadhesive Film: In-vitro, Ex-vivo & In-vivo Investigations

Start date: January 1, 2018
Phase: Phase 1
Study type: Interventional

A total of 24 patients suffering from RAU, they were divided into two groups each included 12 patients. The first group was treated by the propolis mucoadhesive film and the second group received the film without the active component (placebo group).Patients were handed a checklist for monitoring the actual improvement of the clinical parameters which included; duration of disappearance of pain after film application (hours), duration of complete healing of the aphthous ulcer (weeks), onset of ulcer size reduction after film application (days), duration of propolis film adherence onto the oral mucosa (hours) and finally the level of patient satisfaction scaled from 1-10.

NCT ID: NCT03593408 Recruiting - Drug Effect Clinical Trials

Pharmacokinetics of Sedatives and Analgesics During Extracorporeal Membrane Oxygenation (ECMO) Support

Start date: February 8, 2019
Phase:
Study type: Observational

This study will measure plasma concentrations of dexmedetomidine, fentanyl, morphine and midazolam in pediatric patients supported with extracorporeal membrane oxygenation (ECMO) aiming to understand the pharmacokinetics of these drugs in this setting.

NCT ID: NCT03532399 Recruiting - Drug Effect Clinical Trials

Pharmacokinetics of Bivalirudin for Pediatric Anticoagulation

Start date: July 12, 2018
Phase:
Study type: Observational

This study will measure plasma concentrations of bivalirudin in pediatric patients undergoing cardiac catheterization, cardiac surgical procedures utilizing cardiopulmonary bypass (CPB), or extracorporeal support with ECMO, ventricular support devices (VAD) or lung-assist devices (LAD). The aim is to understand the pharmacokinetics of bivalirudin in these settings.

NCT ID: NCT03418714 Completed - Drug Effect Clinical Trials

Effects of Salvinorin A on Brain Function

Start date: December 14, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This study will investigate the effects of salvinorin A on human brain activity and connectivity using functional magnetic resonance imaging (fMRI) methods. An inhalation route of administration will be used as it is the most common route for contemporary use of Salvia divinorum, a plant containing salvinorin A.