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NCT ID: NCT03109327 Completed - Melanoma Clinical Trials

Investigating the Clinical Utility of the MDS

OMS002_UK
Start date: April 1, 2018
Phase:
Study type: Observational

The purpose of this study is to establish the clinical utility of the Melanoma Detection System (MDS).

NCT ID: NCT03115450 Completed - Stroke Clinical Trials

Comparison of Pupilometer and Ultrasound of Optic Nerve Sheath Diameter in Estimating Intracranial Pressure (ICP)

CUSPICP
Start date: April 1, 2018
Phase:
Study type: Observational

The purpose of this investigator-initiated study is to compare the use of pupilometer and ultrasound assessment of optic nerve sheath diameter in predicting the ICP and to see if there is a value that could be used to indicate elevated ICP with either modality as these numbers are inconsistent throughout the literature. Patients that have either an external ventricular drain (EVD) or bolt placed will be enrolled in the study. After the EVD and bolt are placed the patient will undergo pupilometer examination (standard of care) followed by ultrasound assessment of the optic nerve sheath diameter (ONSD). The three values will be recorded. The same patient may have multiple readings performed if there is a change in ICP either spontaneously or due to intervention.

NCT ID: NCT03129243 Completed - Infertility, Male Clinical Trials

Sperm DNA Damage to Intracytoplasmic Sperm Injection Outcome

Start date: April 1, 2018
Phase:
Study type: Observational

In the current era of assisted reproductive techniques where technology can help overcome defects in sperm function, the value of semen analysis has become even more inaccurate. Initial reports of intracytoplasmic sperm injection revealed its ability to bypass the natural selection process and enable men with severely impaired semen parameters to achieve both clinical pregnancy and live birth

NCT ID: NCT03165305 Completed - Clinical trials for Respiratory Distress Syndrome, Newborn

The Role of Sustained Inflation on Short Term Respiratory Outcomes in Term Infants

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

Sustained inflation (SI) has been reported to be effective for reducing the need for intubation and/or invasive ventilation in preterm infants. However, it has also an important role to support the initial breaths and liquid removal from the airways. Therefore, the investigators hypothesized that SI performed just after birth may help to facilitate the transitional period and decrease the incidence of early respiratory morbidities such as transient tachypnea in term infants.

NCT ID: NCT03179046 Completed - Clinical trials for Systemic Lupus Erythematosus

Cardiac and Laboratory Findings in Patients With Systemic Lupus Erythematosus

Start date: April 1, 2018
Phase:
Study type: Observational

This study is designed to investigate the association of the clinical and laboratory parameters or data with the cardiac structural and functional abnormalities in systemic lupus erythematosus(SLE). Patients with at least four ACR classification criteria for SLE and stable clinical condition (no need for immunosuppressive therapy intensification, i.e. current immunosuppressive drug dose increase or introduction of an additional immunosuppressive drug within last 3 months) will be included in the study. Study procedures will include clinical evaluation, lab tests including blood counts, liver and kidney functions and antibodies levels such as ANA, antiphospholipid antibodies, anti-ds DNA as well as inflammatory markers such as sedimentation rates. Also evaluation of cardiac status by cardiologist examination echocardiography and gadolinium enhanced cardiac MRI. Next, correlation between cardiac abnormalities and laboratory changes will be statistically analyzed.

NCT ID: NCT03186261 Completed - Dental Caries Clinical Trials

Antibacterial Effect of Nano Silver Fluoride vs Chlorhexidine on Occlusal Carious Molars Treated With Partial Caries Removal Technique

Start date: April 1, 2018
Phase: Phase 3
Study type: Interventional

- The teeth of the patients that meet inclusion criteria will be anesthetized, isolated with a rubber dam. - Cavity opened using conventional high-speed rotary instruments. - The central cariogenic biomass and the superficial parts of the necrotic dentine will be removed with round burs. - Caries lesion will be completely removed in the enamel/dentin junction. - The excavation procedure will be terminated as soon as the soft and wet dentine was removed and the remaining tissue was leathery but not hard on exploring. - A dentinal sample will then be collected from the base of the cavity using sterile spoon excavator as a baseline for bacteriological assessment. - Then, application of either intervention or control agent, another dentinal sample will be collected using a sterile excavator and transferred into sterile tubes and transferred to the laboratory for microbiological analysis. - Filling of the cavity with resin composite restoration. - All clinical procedures will be carried out at the same visit.

NCT ID: NCT03200028 Completed - Clinical trials for Alcohol Use Disorder

CCTAP: Cognitive Control Training for Treatment of AUD-PTSD

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the feasibility of the revised brain training program with individuals diagnosed with Alcohol Use Disorder (AUD) and Post-Traumatic Stress Disorder (PTSD).

NCT ID: NCT03215121 Completed - Clinical trials for Obstructive Sleep Apnea

Mask Study: One-handed vs. Two Handed Technique in Children

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

During induction of anesthesia in children, the investigators have observed significant variability in mask holding technique at our institution among different anesthesia practitioners. Some hold the face mask using one hand and others use two hands. The aim of our study is to comparatively evaluate the extent of airway obstruction in children whilst anesthetic mask is held with one hand with jaw thrust versus mask held using two hands with chin lift by anesthesia provider during induction of anesthesia in children.

NCT ID: NCT03239392 Completed - CTCL Clinical Trials

A Dose-Ranging Study of IV BNZ-1 in LGL Leukemia or Refractory CTCL

Start date: April 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

This study is an open-label, multi-center, dose-ranging study to characterize the safety, tolerability, preliminary efficacy, and PK/PD of up to four dose levels of BNZ-1 administered weekly by IV infusion to adults diagnosed with Large Granular Lymphocyte (LGL) Leukemia or refractory Cutaneous T-cell Lymphoma (CTCL).

NCT ID: NCT03248687 Completed - Clinical trials for Distal Radius Fracture

Distal Radius Buckle Fracture Follow up Study

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

The investigators will be enrolling children with distal radius buckle fractures, treating them with a removable splint and randomizing them to follow up as needed vs required follow up with a primary care physician 1-2 weeks after the ED visit.