Dr. Stephen Weber Pioneers Safer, More Comfortable Approach to Facial Cosmetic Surgery With Exclusive In-Office Sedation
DENVER, COLORADO / ACCESS Newswire / April 18, 2025 / Dr. Stephen Weber is transforming the surgical experience with his exclusive in-office sedation technique, offering patients a safer, more comfortable and more cost-effective alternative to general anesthesia.
Through years of refinement, Dr. Weber has created a pill-based sedation method that is combined with a specialized, dilute lidocaine numbing solution. This combination ensures patients remain relaxed and pain-free throughout their procedures while avoiding the risks, discomfort, expense and prolonged recovery commonly associated with general anesthesia and other deeper anesthesia techniques.
While Dr. Weber's groundbreaking technique is highly effective for facelifts, neck lifts, liposuction, cheek and chin implants, eyelid surgery, facial implants, fat transfer and ear pinning surgery, it is not suitable for more invasive procedures such as brow lifts or rhinoplasty, which still require traditional anesthesia in a surgical setting. In addition, Dr. Weber maintains ambulatory surgery center and local hospital privileges to accommodate surgery for patients that prefer the traditional general anesthetic approach to his portfolio of facial cosmetic surgery procedures.
Convenience, Cost Savings, and Faster Recovery
By performing procedures in his state-of-the-art office surgery suite, Dr. Weber eliminates the need for a separate ambulatory surgical center, reducing risk, cost and logistical challenges for his patients. Traditional hospital-based surgeries often require additional fees, extended recovery times and unpleasant side effects such as nausea and grogginess from general anesthesia. Dr. Weber's in-office oral sedation technique removes these concerns, offering a streamlined, personalized and more convenient experience.
'Patients love the fact that they can undergo procedures like facelift, neck lift, facial implant procedures, and eyelid surgery in a familiar, private setting,' says Dr. Weber.' They wake up feeling refreshed, without the hangover effect that general anesthesia can cause.'
Dr. Stephen Weber Recognized as a Castle Connolly Top Doctor for 2025
Dr. Stephen Weber, a distinguished Facial Plastic Surgeon, is honored as a Castle Connolly Top Doctor for 2025, a prestigious recognition awarded to the nation's most respected physicians. This accolade highlights Dr. Weber's unwavering commitment to excellence in facial plastic surgery, patient care and surgical innovation. With extensive training and over 15 years of experience, he has earned a reputation for delivering outstanding aesthetic results and pioneering advanced surgical techniques. This and more sets Dr. Stephen Weber apart as a premier cosmetic surgeon, serving patients both from within Denver and abroad.
The Future of Facial Surgery in Colorado
Dr. Weber's commitment to patient safety and comfort has led to a growing number of patients choosing in-office sedation for their procedures. Currently, over 95% of his surgical patients opt for this approach, drawn to its numerous benefits, including:
Dr. Weber is one of only a handful of board-certified Facial Plastic Surgeons worldwide to offer this level of in-office surgical care and is the only Facial Plastic Surgeon in Colorado doing so. Patients say his innovative approach has redefined their comfort, safety and accessibility, making facial cosmetic surgery more convenient than ever.
Contact Information
Dr. Steven Weber
Plastic Surgeon
720-738-4443
SOURCE: Weber Facial Plastic Surgery
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As with any drug development efforts by any company, there can be no assurance at this time that any of the Company's pharmaceutical candidates would show sufficient effectiveness and safety for human clinical development. Further, there can be no assurance at this time that successful results against coronavirus in our lab will lead to successful clinical trials or a successful pharmaceutical product. This press release contains forward-looking statements that reflect the Company's current expectation regarding future events. Actual events could differ materially and substantially from those projected herein and depend on a number of factors. Certain statements in this release, and other written or oral statements made by NanoViricides, Inc. are 'forward-looking statements' within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. You should not place undue reliance on forward-looking statements since they involve known and unknown risks, uncertainties and other factors which are, in some cases, beyond the Company's control and which could, and likely will, materially affect actual results, levels of activity, performance or achievements. The Company assumes no obligation to publicly update or revise these forward-looking statements for any reason, or to update the reasons actual results could differ materially from those anticipated in these forward-looking statements, even if new information becomes available in the future. Important factors that could cause actual results to differ materially from the company's expectations include, but are not limited to, those factors that are disclosed under the heading 'Risk Factors' and elsewhere in documents filed by the company from time to time with the United States Securities and Exchange Commission and other regulatory authorities. Although it is not possible to predict or identify all such factors, they may include the following: demonstration and proof of principle in preclinical trials that a nanoviricide is safe and effective; successful development of our product candidates; our ability to seek and obtain regulatory approvals, including with respect to the indications we are seeking; the successful commercialization of our product candidates; and market acceptance of our products. The phrases 'safety', 'effectiveness' and equivalent phrases as used in this press release refer to research findings including clinical trials as the customary research usage and do not indicate evaluation of safety or effectiveness by the US FDA. FDA refers to US Food and Drug Administration. IND application refers to 'Investigational New Drug' application. cGMP refers to current Good Manufacturing Practices. CMC refers to 'Chemistry, Manufacture, and Controls'. CHMP refers to the Committee for Medicinal Products for Human Use, which is the European Medicines Agency's (EMA) committee responsible for human medicines. API stands for 'Active Pharmaceutical Ingredient'. WHO is the World Health Organization. R&D refers to Research and Development. Public Relations Contact: ir@ View the original press release on ACCESS Newswire The post Measles Cases Increasing Worldwide, Need the New NV-387 Broad-Spectrum Antiviral to Combat, Says NanoViricides appeared first on DA80 Hub.