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Active clinical trials for "Necrosis"

Results 331-340 of 516

Complement Component 3c and Tumor Necrosis Factor-α in Patients With Human Papillomavirus-Induced...

Warts

The investigators explore the role of the complement pathway and T helper 1 immune response in clinical response to Candida immunotherapy via complement component and tumor necrosis factor, respectively.

Completed5 enrollment criteria

INSTANT: INtegrilin Plus STenting to Avoid Myocardial Necrosis Trial

Cardiovascular Disease

Randomized, blind controlled, Multicenter, spontaneous, prospective trial, roughly 20 enrolling centers in Italy, placebo and active drug supply given by GlaxoSmithKline (GSK).

Completed29 enrollment criteria

Endoscopic Ultrasound-guided Drainage of Walled Off Necrosis (WON)

Pancreatic Pseudocyst

The purpose of this study is to compare the effect of lumen-apposing metal stent (LAMS) and double pigtail plastic stents (DPPSs) on the drainage of pancreatic walled-off necrosis (WON), mainly to observe the efficacy and safety of LAMS for WON.

Unknown status14 enrollment criteria

Effect of Diode Laser Activated Irrigation Versus Ultrasonic on Post-Operative Pain in Single Visit...

Necrosis

the investigator intended to study the effect of laser versus ultrasonic in activation of irrigation in post operative pain of patients have a symptomatic necrotic teeth

Unknown status14 enrollment criteria

Effect of BM-MSCs on Early Graft Function Recovery After DCD Kidney Transplant.

Kidney TransplantationAcute Kidney Tubular Necrosis

This study is designed to investigate whether allogeneic bone marrow-derived mesenchymal stem cells (BM-MSCs) can promote function recovery in patients with poor early graft function after kidney transplantation from Chinese Donation after Citizen Death (DCD). DCD kidney transplant recipients with poor early graft function (with or without dialysis) post transplant are equally randomized into MSCs group or control group. Patients in MSCs group are administered MSCs treatment. Allogeneic BM-MSCs (1*10^6/kg) from third party are given intravenously for four consecutive doses every week after enrollment. Patients in control group receive placebo. Renal allograft function (eGFR), rejection, patient/graft survival and severe adverse events up to 12 months post enrollment are monitored.

Unknown status19 enrollment criteria

NANOS Neck Preserving Hip Stem

Primary OsteoarthritisSecondary Osteoarthritis4 more

The objective of this study is to determine the long-term safety and effectiveness of the NANOS neck preserving stem in terms of radiographic and clinical performance as well as short-, mid- and long-term survivorship

Terminated16 enrollment criteria

Trinity™ BIOLOX Delta™ CoC THR Multi-center Study

OsteoarthritisAvascular Necrosis2 more

To demonstrate the safety and effectiveness of the Trinity™ BIOLOX delta™ Ceramic-on-Ceramic Total Hip System in comparison to the Trinity™ Acetabular Hip System,which is FDA cleared for use in the U.S. The comparison will be based upon clinical success at the Month 24 endpoint.

Unknown status27 enrollment criteria

Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder Arthroplasty

OsteoarthritisRheumatoid Arthritis4 more

The objectives of this study are to obtain survival and outcome data on the Trabecular Metal Humeral Stem when used in primary, total or hemi shoulder arthroplasty.

Terminated17 enrollment criteria

Efficacy of Chlorexidine as Intracanal Medicament in Primary Teeth

Dental Pulp Necrosis

The purpose of this study is to evaluate the action of the chlorexidine as intracanal medicament in the reduction of the levels of bacteria inside root canals of primary molar teeth with pulpal necrosis.

Unknown status13 enrollment criteria

Foundation Knee Study - Retrospective

OsteoarthritisPost-traumatic Arthritis3 more

The purpose of this study is to evaluate the use and efficacy of the Encore Foundation Knee System in a group of 200 patients for whom data has already been collected.

Terminated27 enrollment criteria
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