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Necrosis clinical trials

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NCT ID: NCT02037945 Completed - Brain Metastases Clinical Trials

18F-Fluorocholine (18F-FCho) to Distinguish Necrosis From Recurrence in Brain Metastases

Start date: January 2014
Phase: N/A
Study type: Interventional

The main purpose of this study is to determine the distribution of 18F Fluorocholine (18F-FCH) in the brain which can help distinguishing radiation-induced scarring from tumor regrowth. In addition, the study will measure levels of 18F-FCH in the blood and (if applicable) in the brain lesion tissue that is removed as part of the planned brain surgery.

NCT ID: NCT02032147 Completed - Cerebral Necrosis Clinical Trials

Treatment of Cerebral Radiation Necrosis (CRN) With Nerve Growth Factor (NGF)

Start date: March 2009
Phase: N/A
Study type: Observational

Cerebral radiation necrosis (CRN) is a well-documented late complication of radiation therapy for cancers, and may have a devastating effect on the patient's quality of life (QOL). However,CRN was once regarded as a progressive and irreversible disease, no standard therapy has been suggested for CRN. In our clinical practice, we have used nerve growth factor(NGF) to treat CRN, and found that GM1 can successfully reverse CRN. A case report has been published in Journal of Clinical Oncology (JCO) in 2011. So we carried out this prospective study to test the efficacy of NGF for CRN.

NCT ID: NCT02007824 Completed - Pressure Ulcer Clinical Trials

Clinical Trial to Evaluate Ultrasonic Surgical Device in Chronic Pressure Ulcer

Start date: August 2013
Phase: N/A
Study type: Interventional

Study objective The purpose of this trial is to evaluate the efficacy and safety of the investigational device, ULSD-12D, as Compared to the comparator, SONOCA-180, in chronic wound.

NCT ID: NCT01977118 Completed - Acute Pancreatitis Clinical Trials

Use of Streptokinase for Enhancement of Percutaneous Drainage of Pancreatic Necrosis

Start date: May 2013
Phase: Phase 2/Phase 3
Study type: Interventional

Around 20 per cent of patients with acute pancreatitis develop pancreatic or peripancreatic necrosis with or without peripancreatic collection. Percutaneous catheter drainage successfully drains the liquefied component of pancreatic necrosis while the solid component still remains undrained. This infected solid component of pancreatic necrosis is probably responsible for failure of percutaneous catheter drainage which demands surgical debridement. Streptokinase is a protein secreted by several species of streptococci which can bind and activate human plasminogen. In the present study investigators plan to instill streptokinase locally in to the collections of patients with severe acute pancreatitis via pigtail catheter inorder to liquefy the solid necrotic component and analyze whether it hastens the drainage and thereby delays or obviates the need for necrosectomy.

NCT ID: NCT01976065 Completed - Pulp Necrosis Clinical Trials

Regeneration of Pulp-Dentin Development in Teeth With Necrotic Pulps and Immature Roots

Start date: September 2014
Phase: Phase 1
Study type: Interventional

This multi-center exploratory clinical trial is a randomized trial designed to test whether a regenerative endodontic procedure using tissue engineering principles (REGENDO), or a revascularization (REVASC) endodontic procedure, in comparison to standard apexification treatment using a mineral trioxide aggregate barrier (apexification; APEX), produces a significantly better composite clinical outcome for the treatment of immature permanent teeth with pulpal necrosis.

NCT ID: NCT01974869 Completed - Clinical trials for Inflammatory Bowel Diseases

Anti Tumor Necrosis Factor Alpha Agents and Surgical Stress Response

Start date: March 2014
Phase: N/A
Study type: Observational [Patient Registry]

Background: The immunologic response to stress is regulated by the cytokines. Anti-Tumor Necrosis Factor-α agents are antibodies directed against a key cytokine in the process angiogenesis and collagen synthesis. It is not known whether they intervene with surgical stress response increasing the rate of postoperative complications. Method: Un-blinded prospective, non-interventional cohort single centre study including all the patients with Crohn's disease and Ulcerative Colitis undergoing abdominal surgery. Immunological and endocrinological parameters will measured in blood samples taken from these patients before and after surgery. Power calculations showed that 17 patients in each arm are needed.

NCT ID: NCT01903980 Completed - Clinical trials for Epipericardial Fat Necrosis

Epipericardial Fat Necrosis: A Misdiagnosed Condition

epipericardial
Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

Epipericardial fat necrosis is a benign and self-limited condition that mainly curses with acute pleuritic chest pain and therefore must be an important differential diagnosis for patients in emergency department (ED). The knowledge of characteristics symptoms and correct management may avoid misdiagnosis or mistakes with other severe conditions like pulmonary embolism, pericarditis or acute coronary disease. Despite the importance of this entity, only fewer than 40 cases have been reported since 1957, when the condition was first described. We have seen a couple of similar cases in our institution during a short period of time, and we suspect that these numbers doesn`t mean the real prevalence of epipericardial fat necrosis, so maybe this condition could be underdiagnosed. Instead, there isn't a study that tried to estimate an incidence of this entity.

NCT ID: NCT01865201 Completed - Clinical trials for Nasopharyngeal Carcinoma

Effect of Edaravone on Radiation-induced Temporal Lobe Necrosis

Start date: March 2009
Phase: Phase 2
Study type: Interventional

It is hypothesized that excessive generation of free radicals involves in the pathogenesis of radiation-induced brain necrosis. This study therefore evaluated the effect of free radical scavenger, edaravone, on radiation-induced temporal lobe necrosis (TLN) in patients with nasopharyngeal carcinoma (NPC) after radiotherapy.

NCT ID: NCT01827098 Completed - Clinical trials for Dental Pulp Necrosis

A Clinical Study to Compare Two Revascularization Protocols to Treat Non-vital Teeth With Incomplete Root Formation

Start date: October 2012
Phase: N/A
Study type: Interventional

Both methods tested in this study disinfect the non-vital root canals and induce blood clot formation inside the root canal. One method places calcium hydroxide inside the root canal after disinfection and the blood clot is induced four weeks later. The other method performs disinfection and induction of blood clot in one appointment. The investigators hypothesize that both methods will obtain the same success rate in eliminating infection, increase in root length and canal walls thickness.

NCT ID: NCT01820611 Completed - Clinical trials for Rheumatoid Arthritis

Arcos Revision Stem: Evaluation of Clinical Performance

Start date: February 2013
Phase:
Study type: Observational

The primary purpose of this study is to evaluate the clinical performance of the Arcos Revision Stem system, determine the stability of the implants, and evaluate any relationship between Paprosky bone defect level and the success of the Arcos Stem.