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Search / Trial NCT06732921

Recovery Control Tower Feasibility Pilot

Launched by WASHINGTON UNIVERSITY SCHOOL OF MEDICINE · Dec 9, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

The Recovery Control Tower Feasibility Pilot is a study looking at how telemedicine can help patients after elective surgery. This means that instead of always needing to see a doctor in person, patients might be able to have some of their care and follow-up done through video calls or other remote methods. The goal is to see if this approach is not only efficient and safe but also helps improve the recovery experience for patients in the Post-Anesthesia Care Unit (PACU). If this pilot is successful, the researchers plan to expand this method to other hospitals.

To be part of this study, you need to be an adult (18 years or older) who is scheduled for elective surgery at Barnes Jewish Hospital in St. Louis, Missouri. If you join the study, you can expect to receive care that might include using telemedicine tools to check on your recovery after surgery. This pilot study is currently looking for participants, and everyone, regardless of gender, is welcome to apply.

Gender

ALL

Eligibility criteria

  • Adults (18 years and older)
  • Undergoing elective surgery at Barnes Jewish Hospital in St. Louis, Missouri will be enrolled.

About Washington University School Of Medicine

Washington University School of Medicine is a leading academic medical institution renowned for its commitment to advancing healthcare through innovative research, education, and patient care. With a strong emphasis on translating scientific discoveries into practical applications, the institution conducts a diverse array of clinical trials aimed at improving treatment outcomes and enhancing the understanding of various medical conditions. Its collaborative environment fosters partnerships between researchers, clinicians, and community stakeholders, ensuring that the trials not only contribute to scientific knowledge but also address the pressing health needs of diverse populations.

Locations

Saint Louis, Missouri, United States

Patients applied

0 patients applied

Trial Officials

Michael S Avidan, MBBcH

Principal Investigator

Washington University School of Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported