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Study identifier: NCT07060495 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

RADA16 for Adult Tonsillectomy

Condition: Postoperative Pain  ·  Sponsor: Rutgers, The State University of New Jersey

PhasePhase 3
Planned participants134
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of the research is to determine if RADA16 (also known as PuraStat®, PuraGel®, or PuraSinus®) improves patient outcomes following tonsillectomy procedures. Researchers will compare application of device RADA16 to application of no device to see if RADA16 works to treat post tonsillectomy hemorrhage. Participants will: * Undergo tonsillectomy procedure. * Receive and fill out a survey sent via email every 2 days following their procedure for 15 days and track their symptoms.

This description comes directly from the study's public registry record.

Talk to the study team

Wayne D Hsueh, MD  ·  973-972-4588  ·  wayne.hsueh@rutgers.edu

Emily Kwon, BA  ·  esk104@njms.rutgers.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Cooperman Barnabas Medical CenterLivingston, New Jersey, United StatesRecruiting
University HospitalNewark, New Jersey, United StatesNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07060495