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NCT ID: NCT03166384 Completed - Clinical trials for Seroma as Procedural Complication

ELectrosurgical Bipolar Devices VS Conventional Electro-cauterization in Breast Surgery

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

There was no study about application of electrosurgical bipolar sealing device for mastectomy in Korean population, because Korean national insurance did not cover use of the advanced sealing device until last year. Sample size of the previous studies was too small to draw a solid conclusion. Therefore, this study was designed prospectively to evaluate whether application of bipolar energy device for mastectomy could provide clinical benefit in terms of reducing seroma formation.

NCT ID: NCT03166306 Completed - Clinical trials for Pulmonary Arterial Hypertension

Angiogenic Imaging in Pulmonary Arterial Hypertension

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

Pulmonary arterial hypertension (PAH) is a disorder of elevated pulmonary vascular resistance characterized by progressive remodeling and obliteration of vessels of the distal pulmonary circulation. Outcomes in PAH could be improved with earlier diagnosis, and with the early deployment of therapies before irreversible changes have occurred. This study tests the sensitivity of positron emission tomography (PET)-CT scanning with [89Zr]-bevacizumab, a radioisotope-conjugated anti-VEGF antibody for detecting pulmonary vascular remodeling in PAH disease. This test could enable non-invasive diagnosis early in the course of the disease, and potentially improve outcomes in PAH,

NCT ID: NCT03166267 Completed - Tibial Fractures Clinical Trials

Real Life Weight Bearing After Tibial Fractures

Start date: May 24, 2018
Phase:
Study type: Observational

In this prospective case series patients with a tibial fracture are monitored with smart biofeedback systems to document the healing progression and real life weight.

NCT ID: NCT03166215 Completed - Clinical trials for Developmental and/or Epileptic Encephalopathies

Study of TAK-935 as an Adjunctive Therapy in Participants With Developmental and/or Epileptic Encephalopathies

Start date: August 17, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to characterize the multiple-dose safety and tolerability profile of TAK-935 in adult participants with developmental and/or epileptic encephalopathies.

NCT ID: NCT03165851 Completed - Clinical trials for Acute Myeloid Leukemia, Pediatric

Efficacy Analysis of Comparison of CAMS(Chinese Academy of Medical Sciences)-2005 Trial and CAMS-2009 Trial for Pediatric Acute Myeloid Leukemia

Start date: April 10, 2005
Phase: N/A
Study type: Observational

The investigators adopted the CAMS(Chinese Academy of Medical Sciences)-2009 trial for pediatric acute myeloid leukemia (AML) patients between 2009 to 2015, in which a risk-stratified strategy and dose-dense intensive chemotherapy were introduced. The outcomes of CAMS-2009 trial were retrospectively analyzed, and compared to the CAMS-2005 trial.

NCT ID: NCT03165773 Completed - Clinical trials for Glycemic and Insulinemic Response

Four-hour Glycemic Kinetic Response Following 13C-enriched Oatmeal Breakfast Compared to Hot Corn Grits

Start date: August 24, 2015
Phase: N/A
Study type: Interventional

The objectives of this study are to assess the 4 hr postprandial kinetics of total and exogenous glucose in response to consumption of oatmeal containing a high percentage of the viscous agent β-glucan, in comparison to a β-glucan free corn cereal that is matched by grams of available carbohydrate.

NCT ID: NCT03165760 Completed - Clinical trials for Postoperative Complications

Protective Mechanical Ventilation and Risk of Postoperative Complications in Abdominal Surgery

Start date: July 1, 2015
Phase: N/A
Study type: Interventional

Randomized controlled trial, comparing two groups of 40 patients each scheduled for open major abdominal surgery. The intervention group was ventilated with a protective strategy consisting on a low Tidal volume (Vt) (6ml/kg of predicted body weight (PBW)), positive end expiratory pressure (PEEP) = 10 cm H2O and recruitment manoeuvres (RM) after disconnection from the ventilator, the control group had classic ventilation (Vt = 8 ml/kg of PBW, PEEP = 4 cmH2O and no RM).

NCT ID: NCT03165656 Completed - Clinical trials for High Altitude Pulmonary Hypertension

Right Ventricular Function at Rest in Highlanders/Lowlanders

Start date: May 24, 2017
Phase:
Study type: Observational [Patient Registry]

The purpose of the current study is to evaluate the progression of right ventricular function and dimension in Kyrgyz highlanders with high altitude pulmonary hypertension (HAPH) by performing a cross sectional case-control study.

NCT ID: NCT03165526 Completed - Clinical trials for Post-Infarction Ventricular Septal Defect

The AMPLATZER™ Post-infarct Muscular VSD Occluder Humanitarian Device Exemption (H070005) Post Approval Study

PIVSD PAS
Start date: October 1, 2018
Phase:
Study type: Observational

FDA issued a Humanitarian Device Exemption (HDE) approval order for the AMPLATZER™ PIVSD Occluder (H070005) on January 10, 2017. The Conditions of Approval require that SJM conduct a post approval study to evaluate the safety and probable benefit of the AMPLATZER™ PIVSD Occluder.

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.