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NCT ID: NCT03250845 Completed - Clinical trials for Hematologic Diseases

Comparison of Multigam IV (5% vs. 10%) in Patients With an Immunodeficiency Secondary to a Hematological Disorder

MULTISIM
Start date: June 30, 2017
Phase:
Study type: Observational

The purpose of this observational study is to compare the administration of standard of care Multigam IV 5% and standard of care Multigam IV 10% in order to observe changes in infusion time and infusion related reactions. Patient satisfaction, number of actions taken by the nursing staff during infusion and satisfaction of the nursing staff will also be evaluated.

NCT ID: NCT03249974 Completed - Clinical trials for Type1 Diabetes Mellitus

Comparison Between Enlite and Flash Glucose Monitoring

Start date: July 5, 2017
Phase:
Study type: Observational

1. The accuracy of the sensors (Flash vs Enlite glucose monitoring) will be evaluated with a standardized breakfast test. Patients receive a standardized breakfast. The usual insulin bolus will be administered at breakfast. After breakfast, a venous blood sample is taken for 2 hours every 15 minutes to determine the blood sugar. At the same time, the glucose value shown by the sensors will be noted. A comparison of the blood glucose value with the data recorded by the sensor can evaluate the accuracy of the sensor and also estimate the lag-time between the sensor glucose and the venous glucose. 2. Patient satisfaction will be evaluated using a questionnaire that will be completed after the Enlite sensor has been worn for 1 month. 3. The development of skin reactions will be checked by a short questionnaire, supplemented with a picture of possible skin phenomena. 4. The data recorded by the FreeStyle sensor (average glucose,% above target,% within target,% under target, amount of hypoglycemia) in the month prior to sensor switching will be compared to the same data recorded by the Enlite sensor during the first month of use.

NCT ID: NCT03249402 Completed - Healthy Clinical Trials

A Study to Evaluate the Effect of Multiple Oral Doses of JNJ-42847922 on the Steady-state Pharmacokinetics of an Oral Contraceptive Containing Ethinyl Estradiol and Levonorgestrel in Healthy Female Adult Participants

Start date: August 14, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the effect of multiple 40 milligram (mg) doses of JNJ-42847922 on the steady state pharmacokinetics (PK) of multiple doses of a combination oral contraceptive (OC) containing ethinyl estradiol (EE) and levonorgestrel (LN) in healthy female adult partcipants.

NCT ID: NCT03248908 Completed - Anesthesia Clinical Trials

Pupillary Dilation Reflex Assessment for Intraoperative Analgesic Titration.

PUP-AIT
Start date: October 12, 2017
Phase: N/A
Study type: Interventional

In this double blinded randomized controlled study, the pupillary dilation reflex is used for as a nociceptive indicator for opioid administration during elective surgery under general anesthesia.

NCT ID: NCT03248531 Completed - Clinical trials for Hidradenitis Suppurativa

A Study to Test the Efficacy, Safety and Pharmacokinetics of Bimekizumab in Subjects With Moderate to Severe Hidradenitis Suppurativa.

Start date: September 22, 2017
Phase: Phase 2
Study type: Interventional

Hidradenitis suppurativa (HS) is a painful, long-term skin condition that causes abscesses and scarring on the skin.

NCT ID: NCT03245268 Completed - Clinical trials for Chronic Thromboembolic Pulmonary Hypertension

International BPA Registry

Start date: March 2, 2018
Phase:
Study type: Observational [Patient Registry]

The International Balloon Pulmonary Angioplasty (BPA) Registry is a prospective, multi-center, long-term observational project. Scheduled to start data collection in Q4 2017, the registry will run for approximately four years with a follow-up time for each patient of at least two years. Its primary objective is to investigate the efficacy and safety of BPA intervention in patients with chronic thromboembolic pulmonary hypertension (CTEPH) not amenable to pulmonary endarterectomy (PEA).

NCT ID: NCT03244514 Completed - Clinical trials for Acute Kidney Injury (Nontraumatic)

Biomarker-guided Implementation of the AKI Bundle

PrevAKI-mc
Start date: November 2, 2017
Phase: N/A
Study type: Interventional

There is no specific therapy for acute kidney injury. It is presumed that supportive measures improve the care and outcome of patients with acute kidney injury. The investigators hypothesize that the implementation of a bundle of supportive measures adapted to patients undergoing cardiovascular surgery reduces the occurence of AKI. A Randomized prospective multicenter trial is needed to investigate whether the implementation of the bundle of measures is effective to prevent AKI in high risk patients undergoing cardiac surgery. In this feasibility trial the investigators will analyze the compliance rate to the trial protocol in a multicenter, multinational cohort in preparation for a large randomized controlled trial.

NCT ID: NCT03244332 Completed - Child, Only Clinical Trials

HEMOCC Study. Hemostasis in Cirrhotic Children.

HEMOCC
Start date: October 18, 2013
Phase: N/A
Study type: Interventional

Prospective investigations into the role of hemostatic factors in the risk of variceal bleeding among children with chronic liver disease (thromboelastometry e.g) is still required. A better understanding of these factors would permit better risk stratification and targeted prophylaxis or therapy.

NCT ID: NCT03243669 Completed - Colonic Adenoma Clinical Trials

High Definition Endoscopy and Virtual Chromoendoscopy Versus Standard Resolution Endoscopy in Detection of Colon Polyps

Start date: December 1, 2010
Phase: N/A
Study type: Interventional

Over the last years a number of new endoscopic imaging modalities have been introduced (high-definition and virtual chromoendoscopy). Given the theoretical advantage of these new imaging techniques, the investigators aimed to investigate their use for the detection of polyps during colonoscopy.

NCT ID: NCT03241134 Completed - Clinical trials for Work-Related Condition

Changes in Surface EMG Activity After Dry Needling Compared to Sham Needling

Start date: August 28, 2017
Phase: N/A
Study type: Interventional

An experimental study will be conducted to evaluate the effect of a single dry needling session, compared to a sham needling session, on surface EMG activity (signal amplitude and frequency) and pain of the upper trapezius muscle, in office workers with trapezius myalgia.