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Necrosis clinical trials

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NCT ID: NCT03930173 Completed - Clinical trials for Secondary Malignant Neoplasm of Brain and Cerebral Meninges

18F-Fluciclovine PET to Distinguish Tumor Progression From Radiation Necrosis

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

The purpose of this study is to evaluate whether 18F-fluciclovine PET/CT of the brain, is able to distinguish radiation necrosis from tumor progression in cases where MRI is inconclusive. 18F-fluciclovine is an FDA approved radioactive diagnostic agent and is injected into the participant and then taken up by cancer cells, which can then be visualized with a PET/CT scan. 18F-fluciclovine is FDA approved for the detection of recurrent prostate cancer, but is still investigational for the purposes of this study.

NCT ID: NCT03923686 Completed - Clinical trials for Pancreatitis, Acute Necrotizing

Lumen-apposing Metal Stent With or Without Coaxial Plastic Stent for Treatment of Walled-off Pancreatic Necrosis

Start date: May 13, 2019
Phase: N/A
Study type: Interventional

A prospective randomized cohort study to compare whether the placement of a double-pigtail plastic stent (DPS) within a lumen-apposing metal stent (LAMS) may improve the efficacy and safety of endoscopic ultrasound guided transmural drainage of walled-off pancreatic necrosis (WON) and thus prevent potential adverse events related to LAMS insertion.

NCT ID: NCT03910205 Completed - Clinical trials for Periodontal Diseases

Tumor Necrosis Factor-alpha and Interleukin-18 Levels in Children With Gingivitis and Type 1 Diabetes Mellitus

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

This study aimed to evaluate the levels of interleukin 18 and tumor necrosis factor-alpha (TNF-α) in gingival crevicular fluid (GCF) of children with type 1 diabetes mellitus and gingivitis.

NCT ID: NCT03860493 Completed - Clinical trials for Perfusion; Complications

Feasibility of the IC-Flow Device for Fluorescent Perfusion Evaluation During Feasibility of the IC-Flow Device

IC-Flow
Start date: May 15, 2019
Phase:
Study type: Observational

1. Primary Objective: Demonstrate that the IC-Flow Imaging device with Indocyanine Green (ICG) is a feasible technique when visualizing and identifying perfusion of organs when compared to The KARL STORZ VITOM II ICG System during open reconstructive surgical procedures 2. Secondary Objective: 1. Evaluate the mean Assessment of handling properties using The IC- Flow versus The VITOM II. 2. Evaluate the mean Surgeon preference Level using The IC- Flow tower, The IC-Flow Hand-held device versus The VITOM II.

NCT ID: NCT03849222 Completed - Pulp Necrosis Clinical Trials

Evaluation the Effect of Using of Apical Matrix With Apexification Procedure on Apical Healing of Necrotic Immature Teeth

Start date: August 20, 2013
Phase: Phase 2/Phase 3
Study type: Interventional

This study was conducted to evaluate the effect of the use of apical matrix, with Mineral Trioxide Aggregate (MTA) or calcium hydroxide Ca(OH)2 Apexification on apical healing and calcific barrier formation of immature teeth with non- vital pulp.

NCT ID: NCT03813433 Not yet recruiting - Pulp Necrosis Clinical Trials

Discoloration of Endosequence and Mineral Trioxde Aggregate in Revascularization of Necrotic Immature Permanent Teeth

Start date: June 2023
Phase: N/A
Study type: Interventional

the objective of this study is to evaluate post operative pain after using Endosequence versus Mineral Trioxide Aggregate as coronal plug material in revascularization of non vital immature anterior teeth

NCT ID: NCT03808272 Completed - Clinical trials for Pancreatic Pseudocyst and Walled-off Necrosis

AXIOS CHINA (E7148)

Start date: April 17, 2019
Phase: N/A
Study type: Interventional

To study the safety and effectiveness of the AXIOS Stent with Electrocautery Enhanced Delivery System for endoscopic trans enteric drainage of pancreatic pseudocyst and walled-off necrosis in Chinese population, to support the regulatory approval by CFDA

NCT ID: NCT03806842 Active, not recruiting - Rotator Cuff Tear Clinical Trials

Easytech Reversed Shoulder System Clinical Study

Start date: November 28, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to collect data to demonstrate the safety and effectiveness of the Easytech Reversed Shoulder System for the treatment of patients who require a reverse total shoulder arthroplasty.

NCT ID: NCT03804450 Completed - Pulp Necroses Clinical Trials

Magnetic Resonance Imaging (MRI) of Pulp Regeneration

Start date: July 1, 2017
Phase: Phase 2
Study type: Interventional

The present study was conducted to test whether pulp-like tissue can be regenerated in mature teeth with closed apex? And whether the size of the apical diameter affects the success of REPs? And whether Magnetic resonance imaging (MRI) can be used to quantitatively assess the vitality of the regenerated pulp-like tissue.

NCT ID: NCT03801070 Completed - Clinical trials for Walled Off Pancreatic Necrosis (WON)

Rad Predictors for WON

Start date: July 14, 2017
Phase:
Study type: Observational

This is a retrospective chart review study examining 1) demographic data such as age, sex, etiology of pancreatitis 2) clinical data including radiological characteristics of walled off pancreatic necrosis, walled off necrosis related admissions and readmission following endoscopic drainage, surgical or percutaneous procedures performed for the management of walled off pancreatic necrosis, and clinical outcomes following treatment of WON (including hospital readmissions, WON resolution, procedure complications, WON related death) 3) endoscopy data including indication for initial endoscopic drainage and subsequent endoscopic procedures performed for management of walled off necrosis (including additional EGD's, endoscopic drainage procedures, and/or necrosectomy)