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Treating Intraoperative Bradycardia in Non-cardiac Surgery Patients With Atropine at Heart Rates Below 60 Versus 30 Beats Per Minute and Norepinephrine Requirements

Launched by UNIVERSITY OF HAMBURG-EPPENDORF · Apr 9, 2025

Trial Information

Current as of July 27, 2025

Recruiting

Keywords

ClinConnect Summary

The RAPID trial is a study designed to find out how effective atropine is in treating a condition called intraoperative bradycardia, which means a slow heart rate during surgery. Specifically, the trial will compare giving atropine when the heart rate is below 60 beats per minute to giving it only when the heart rate drops below 30 beats per minute. Researchers want to see if this approach can reduce the need for norepinephrine, a medication used to raise blood pressure during surgery, in patients who are undergoing non-cardiac surgeries that last at least an hour.

To participate in this trial, patients must be at least 50 years old and scheduled for elective non-cardiac surgery with general anesthesia. They should also have at least two risk factors for developing kidney problems, such as being 65 or older, having high blood pressure, or diabetes. It’s important to note that some patients may not be eligible if they have certain health issues that make it unsafe for them to receive atropine. Participants in the trial will receive careful monitoring during their surgery to ensure their heart rate and blood pressure are managed safely.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria: Consenting patients ≥50 years scheduled for elective non-cardiac surgery with general anesthesia that is expected to last ≥60 minutes with at least two of the following risk criteria for developing acute kidney injury:
  • Age ≥65 years
  • American Society of Anesthesiologists physical status III or IV
  • Chronic arterial hypertension
  • Diabetes mellitus requiring medication
  • Intraabdominal surgery
  • Preoperative renal insufficiency (serum creatinine ≥1.2 mg/dL)
  • Exclusion Criteria:
  • Patients with the following exclusion criteria: contraindication for atropine administration (e.g., myasthenia gravis, high-grade aortic stenosis, high-grade coronary artery disease, glaucoma, paralytic ileus, prostatic hypertrophy); renal replacement therapy within the previous 3 months; chronic kidney disease with an estimated glomerular filtration rate \<20 mL/min/1.73 m2; pregnancy.

About University Of Hamburg Eppendorf

The University of Hamburg-Eppendorf (UKE) is a prominent academic medical center in Germany, renowned for its commitment to advancing healthcare through innovative research and education. As a leading clinical trial sponsor, UKE integrates cutting-edge scientific inquiry with clinical practice, fostering a multidisciplinary approach to health challenges. The institution is dedicated to conducting high-quality clinical trials that adhere to rigorous ethical standards, promoting patient safety and contributing valuable insights to the medical community. With a focus on collaboration and excellence, UKE aims to translate research findings into effective therapeutic strategies, ultimately enhancing patient outcomes and public health.

Locations

Hamburg, , Germany

Patients applied

0 patients applied

Trial Officials

Alina Bergholz, MD

Principal Investigator

University Medical Centre Hamburg-Eppendorf

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported