CI

At a glance

ClinicalIndex Comparison Record
N/ANot Yet Recruiting· 100 target
Drug / intervention
Intravenous caffeine +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05464940
NCT05464940N/ANot Yet Recruiting

Impact of Intravenous Caffeine on Atrial Electrical Properties and Potential Arrythmia Induction in Patients With Paroxysmal Atrial Fibrillation: The COFFEE-AF Trial

Kansas City Heart Rhythm Research Foundation·interventional·Posted Jul 19, 2022·Updated Aug 28, 2025

In Brief

A clinical study evaluating Intravenous caffeine and Masked Placebo for Atrial Fibrillation. Not yet recruiting, targeting 100 participants across 9 sites.

Detailed Summary

This "How caffeine Induces Atrial Tachyarrhythmias" trial will be a multi-center, randomized, double-blinded trial of intravenous caffeine versus placebo among patients undergoing pulmonary vein isolation procedures for Atrial Fibrillation(AF).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

N/ANot Yet RecruitingOverdue
2023202420252026
First PostedJul 19, 2022
Enrollment StartSep 1, 2025
Primary CompletionMar 1, 2026
Study CompletionJun 1, 2026
TodayJul 1, 2026
Enrollment to primary: 6 monthsPosted 3.9 years ago

Interventions

Intravenous caffeineother

Group assigned to receive caffeine will receive intravenous(IV) caffeine and sodium benzoate infusion starting at 250-500 mg. This method will use an automated algorithm that adjusts the flow of the infusion depending on the individual's sex and weight and then in a serial fashion in response to blood caffeine measurements. Serial blood caffeine measurements at pre-determined intervals according to the algorithm will be until a steady state is obtained.

Masked Placeboother

The patients assigned to the masked placebo will receive 5% dextrose in 0.45% saline using the same infusion protocol for a random length of time that was within 1 standard deviation(SD) of the mean time to achieve a steady state using the caffeine protocol (17+4 min). To maintain blinding, caffeine blood concentration measurements that will be randomly generated within 2 SDs of the predicted values calculated by the algorithm will be used and verbally communicated for placebo infusions.