killocape.blogg.se - Are there any free clinical trials in the chattanooga tn

to maintain the shape of the eye, to cover surgical instruments and to protect the corneal endothelium from damage. Hydrogels of sodium hyaluronate have been used for many years in ophthalmic surgery in Europe and the U.S. To further maximize patient comfort, the pH of VISMED® is adjusted to 7.3, similar to that of the natural tear film. Some preservatives are known to cause toxic or allergic reactions, the symptoms of which include stinging, burning and redness of the eyes. without causing superficial punctate keratitis). As a result, it is non-irritating to ocular tissues and can be used frequently and for extended periods without harming the surface of the eye (e.g. VISMED® is completely free of preservatives. This, together with the coating properties of sodium hyaluronate, results in an increased pre-corneal residence time and tear film break-up time (BUT) and therefore longer lubrication of the eye surface. Sodium hyaluronate also possesses mucoadhesive properties and the ability to entrap water, thus resembling tear mucus glycoprotein. It is believed that this protective coating of the surface of the eye helps prevent dryness and irritation. This means that VISMED® has a high viscosity between blinks and a low viscosity during blinking ensuring efficient coating of the surface of the eye.

Its main physical characteristic is viscoelasticity. Sodium hyaluronate is a natural polymer which is also present in the structures of the human eye. The proprietary formulation contains a highly purified specific fraction of sodium hyaluronate. VISMED® is currently marketed in Europe under the CE mark as a viscoelastic lubricant eye drop.

Why Should I Register and Submit Results?.

More diverse representation in trials is needed to gain insight that will make medicines most effective for all that may have a need for them. In addition, due to the underrepresentation of minorities in clinical trials, CMR has taken the approach to increase enrollment of the diverse populations in our community. Our entire clinical team is committed to producing highly effective and efficient data in an effort to facilitate FDA approval and bring new treatment options to the market. Our center is a well known research center in the local community, surrounding areas and the pharmaceutical industry, due to its reputation for having extensively trained employees who are highly dedicated and devoted in providing the highest standards of patient care at all times. We are dedicated to achieving excellence in the quality of science, providing the best possible research experience for sick and healthy subjects alike and enforcing the highest standards of biomedical ethics for the conduct of research.

Our facility conducts Phase II-IV clinical trials. Our research team consist of a group of Board Certified OB-GYN and Internal Medicine Investigators, Physician Assistant, ACRP Certified Clinical Research Coordinators, Quality Assurance Specialist (ACRP Certified) and Data Entry Specialist. CHATTANOOGA MEDICAL RESEARCH, LLC (CMR) CMR is a privately owned multi-specialty clinical research facility.