search

Active clinical trials for "Necrosis"

Results 141-150 of 516

AVANTAGE® RELOAD Double Mobility Acetabular Cup -Clinical Study

Primary OsteoarthritisPost-Traumatic Arthritis6 more

This is a Post Marketing Clinical Follow Up study (PMCF) on the AVANTAGE RELOAD dual mobility system cup.

Active24 enrollment criteria

A Clinical Evaluation of a Honey Impregnated Dressing at Removing Necrotic Tissue From Chronic Wounds...

Wound HealNecrotic Tissue Removal

The purpose of this study is to evaluate the effectiveness of a honey-impregnated wound dressing at removing necrotic tissue in subjects with chronic foot or ankle wounds.

Terminated24 enrollment criteria

G7 BiSpherical Acetabular Shell PMCF Study

Rheumatoid ArthritisOsteoarthritis6 more

The primary objective of this study is to obtain implant survivorship and clinical outcomes data for the commercially available G7 BiSpherical Acetabular Shell.

Active24 enrollment criteria

Prospective Study for the Evaluation of the Cementless Anatomic Femoral Stem Minimax -Launay

Primary OsteoarthritisSecondary Osteoarthritis6 more

This is a post-marketing surveillance on MiniMAX Stem

Active15 enrollment criteria

ROSA Total Knee Investigational Testing Authorization Study

Knee PainChronic Osteoarthritis4 more

This is a prospective, single-center clinical study designed to facilitate the collection and evaluation of workflow efficiency, patient pain and function, and adverse event data. This clinical study will include Persona Total Knee components using the ROSA Total Knee Robotic System or conventional instrumentation.

Terminated12 enrollment criteria

Corin MiniHip and Trinity Cup Clinical Surveillance Study

Total Hip ArthroplastyOsteoarthritis5 more

The aim of the study is to provide long term follow up data on the performance and safety of the Corin MiniHip and Trinity acetabular cup over a 10-year period.

Active23 enrollment criteria

Pyrocarbon Clinical Follow-up Study

Osteoarthritis of the ShoulderAvascular Necrosis1 more

The objective of this multi-center study is to collect medium and long-term data on the related clinical complications and functional outcomes of the Pyrocarbon Humeral Head to demonstrate safety and performance, in subjects from the Pyrocarbon IDE Study cohort. Data collected from this study will support post-market surveillance and MDR requirements as well provide the basis for peer-reviewed publications on mid- and long-term product performance and safety (five to ten years post-op).

Active4 enrollment criteria

SCP Hip Outcomes Study

Subchondral CystsSubchondral Bone Edema5 more

Post-market clinical outcomes study to collect data on the short- and long-term outcomes for subjects who are undergoing or have undergone the Subchondroplasty® (SCP®) Procedure in the hip in a standard clinical setting. Outcomes to be assessed include medication usage, pain, function, activity levels and patient satisfaction.

Active12 enrollment criteria

Prospective Clinical 5-year Follow-up of the LINK® Endo-Model® SL®

Bone NecrosisArthritis/Arthrosis1 more

The objective of this study is to collect outcome information on patients requiring Total Knee Replacement (TKR) in primary or revision cases and therefore receiving the LINK® Endo-Model® SL® under routine conditions.

Active11 enrollment criteria

Acute Myocardial Necrosis and Depression: Antiplatelet Effect of Reuptake Inhibition of Serotonin...

DepressionCoronary Artery Disease

Primary purpose: To evaluate the evolution in time of the antiaggregant platelet effect of sertraline (SSRI) compared to placebo in depressive patients with ACS (Acute Coronary Syndrome) and treated as recommended by a double antiplatelet therapy, aspirin and clopidogrel. Hypothesis: The benefits of SSRIs observed in depressive patients with ACS are related to an antiplatelet effect.

Terminated32 enrollment criteria
1...141516...52

Need Help? Contact our team!


We'll reach out to this number within 24 hrs