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Search / Trial NCT03997838

Evaluate the Efficacy and Safety of VVZ-149 Injections for the Treatment of Post-Operative Pain Following Abdominoplasty

Launched by VIVOZON, INC. · Jun 20, 2019

Trial Information

Current as of June 18, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Men and women between 18-70 years old, inclusive. Female subjects must meet additional criteria according to childbearing potential.
  • Planning to undergo abdominoplasty
  • Ability to provide written informed consent
  • Ability to understand study procedures and communicate clearly with the investigator and staff
  • American Society of Anesthesiologists (ASA) risk class of I to II.
  • Exclusion Criteria:
  • Emergency or unplanned surgery
  • Previous abdominoplasty
  • Pre-existing condition causing preoperative pain around the site of surgery
  • Women who are pregnant or breastfeeding
  • Chronic pain diagnosis and ongoing or frequent use of pain medications

About Vivozon, Inc.

Vivozon, Inc. is a biopharmaceutical company dedicated to advancing innovative therapies for the treatment of complex diseases. With a strong emphasis on research and development, Vivozon focuses on leveraging cutting-edge science and technology to address unmet medical needs. The company is committed to conducting rigorous clinical trials that ensure the safety and efficacy of its product candidates, fostering collaboration with healthcare professionals, regulatory bodies, and the scientific community. Vivozon aims to improve patient outcomes and enhance quality of life through its pioneering therapeutic solutions.

Locations

San Antonio, Texas, United States

Dayton, Ohio, United States

Anaheim, California, United States

Phoenix, Arizona, United States

Salt Lake City, Utah, United States

Patients applied

0 patients applied

Trial Officials

Doo Lee, PhD

Study Chair

Vivozon, Inc.

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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