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Necrosis clinical trials

View clinical trials related to Necrosis.

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NCT ID: NCT02951741 Completed - Clinical trials for Avascular Necrosis of Hip

Revision Total Hip Replacement Arthroplasty and Hematologic Variables

Start date: April 2015
Phase: N/A
Study type: Observational

Revision total hip replacement arthroplasty is a surgery having intra- and postoperative substantial blood loss. The investigators will investigate the relationship between the various hematologic variables and postoperative bleeding volume.

NCT ID: NCT02946099 Completed - Clinical trials for Dental Pulp Necrosis

Comparison Between Reciproc and Protaper Next

Start date: November 2016
Phase: N/A
Study type: Interventional

Comparing the postoperative pain resulting after mechanical instrumentation using Reciproc reciprocating files versus that resulting after using ProTaper Next rotary files in asymptomatic necrotic molars.

NCT ID: NCT02929511 Completed - Clinical trials for Apical Periodontitis

Reciprocation vs Rotational Single-file Systems in Postoperative Pain

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

In this study, the researchers will investigate the effect of single-file reciprocating versus single-file rotational file systems on the postoperative pain in adult patients who have necrotic pulp and apical periodontitis. The participants will be assigned by chance to separate groups that compare 2 different treatments, reciprocating single-file system (Reciproc Blue) and rotational single-file system (OneShape). As a reference, Mtwo multi-file (full-sequence) will be used.

NCT ID: NCT02927522 Recruiting - Clinical trials for Rheumatoid Arthritis

Donepezil Attenuate Postoperative Cognitive Dysfunction

DAPOCD
Start date: September 1, 2018
Phase: Phase 3
Study type: Interventional

Postoperative cognitive dysfunction (POCD) occurs mainly in aged patients. POCD may increase the mortality and morbidity. However, the mechanism of POCD is not clear yet and no effective therapy method was proved. According to our previous study, the central cholinergic system impaired by the anesthesia and surgery play a very important role in the POCD and donepezil an acetylcholinesterase inhibitor can prevent the POCD after isoflurane anesthesia in aged mice. Donepezil is a commercial medicine used for the Alzheimer Disease, which is tolerable and has minimal adverse events. In present study a multi-center randomized case control study was conducted and we hypothesized that donepezil attenuate the POCD.

NCT ID: NCT02907489 Completed - Clinical trials for Asymptomatic Necrotic Teeth

Effect of Triple Antibiotic Paste as an Intracanal Medication With an Anti-Inflammatory Drug on Post-operative Pain.

Start date: October 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether the use of triple antibiotic paste as intracanal medication with an anti-inflammatory drug, compared to a calcium hydroxide will reduce postoperative pain and intracanal bacteria or not in patients with asymptomatic necrotic teeth.

NCT ID: NCT02889575 Completed - Acute Renal Failure Clinical Trials

Predictive Value of PIIINP and Urinary NGAL in Renal Function Recovery

PIIINP-NGAL
Start date: April 2012
Phase: N/A
Study type: Observational

Acute Renal Failure (ARF) is defined by a severe, and usually reversible, glomerular filtration rate decreasing. Acute Tubular Necrosis (ATN) remain the major cause of ARF involving distress and destruction of tubular cells. This specific typology of ARF may evolve toward Chronic Renal Failure (CRF) concretizing a major public health issue. Predict the progression of ARF towards CRF appears essential. The investigators believe that the PIIINP and urinary NGAL biomarkers may constitute robust biomarkers of progression risk towards CRF.

NCT ID: NCT02877472 Recruiting - Clinical trials for Femoral Neck Fracture

Porous Tantalum Rods Improve the Hip Joint Function of Patients With Avascular Necrosis of the Femoral Head

Start date: May 2015
Phase: N/A
Study type: Interventional

To confirm 1) whether, compared with core decompression alone, core decompression with porous tantalum rod implantation improves the hip joint function of patients with avascular necrosis of the femoral head after femoral neck fracture surgery, 2) whether porous tantalum rod shows favorable biocompatibility with the human body, and 3) whether this treatment method is feasible for treating avascular necrosis of the femoral head after femoral neck fracture surgery.

NCT ID: NCT02862574 Terminated - Clinical trials for Rheumatoid Arthritis

Andecaliximab as Add-On Therapy to a Tumor Necrosis Factor Inhibitor and Methotrexate Regimen in Adults With Moderately to Severely Active Rheumatoid Arthritis

Start date: December 15, 2016
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of andecaliximab (GS-5745) versus placebo as an add-on therapy to a tumor necrosis factor (TNF) inhibitor and methotrexate in adults with moderate to severe rheumatoid arthritis (RA).

NCT ID: NCT02819479 Completed - Radiation Necrosis Clinical Trials

Low-dose Intra-arterial Bevacizumab for Edema and Radiation Necrosis Therapeutic Intervention (LIBERTI)

LIBERTI
Start date: November 23, 2016
Phase: Phase 2
Study type: Interventional

To assess the overall safety and efficacy of intra-arterial (IA) bevacizumab for the treatment of radiation necrosis. A single 2.5 mg/kg dose of bevacizumab will be given intra-arterially after osmotic blood-brain-barrier disruption.

NCT ID: NCT02799654 Withdrawn - Hip Fractures Clinical Trials

Excia T Cementless EBRA Study

Start date: August 2017
Phase: N/A
Study type: Observational

In this Post Market Clinical Follow-up Study (PMCF Study), the short-term clinical and radiological results of the cementless Excia T® prosthesis in routine clinical use shall be assessed and the migration taking place in the first 24 months evaluated.