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Diltiazem in the Treatment of Atrial Fibrillation or Atrial Flutter With Rapid Ventricular Rate (AFF RVR)

Primary Purpose

AFF With RVR, Atrial Fibrillation With Rapid Ventricular Response (Disorder), Hypotension Drug-Induced

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Calcium pre-treatment
No Intervention
Sponsored by
Aurora Health Care
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for AFF With RVR focused on measuring diltiazem, calcium

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age > 18 years or older Able to provide informed consent Primary diagnosis AFF with RVR greater than or equal to 120 bpm Exclusion Criteria: Pregnancy defined as a positive urine HCG Hemodynamically unstable patients (SBP <90, MAP <65) Stated history of systolic heart failure with reduced ejection fraction (<40%) or evidence of acute heart failure or reduced EF (peripheral edema, JVD, pulmonary edema) on clinical exam or bedside echo Patients with left ventricular assist device Sinus node dysfunction or preexcitation with accessory pathway (known diagnosis of SVT, WPW or sick sinus syndrome. Delta waves or other evidence of accessory pathway on EKG) 2nd or 3rd degree atrioventricular block Allergy or sensitivity to any study drugs Previously enrolled in this trial during a different patient encounter Non-English speaking

Sites / Locations

  • Advocate Christ Medical Center Emergency Department (ACMC ED)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Calcium pre-treatment

Placebo

Arm Description

Calcium gluconate 1 gram/100ml 0.9% NaCl or 100ml 0.9% NaCl

diluent (NS) vials

Outcomes

Primary Outcome Measures

Mean Difference in SBP
The primary endpoint is the Mean difference in SBP evaluated at 5 and 15 minutes after administration of diltiazem bolus. Monitors were set to obtain an automated full set of vitals every 5 minutes after administration of diltiazem.

Secondary Outcome Measures

Mean change in heart rhythm
Secondary endpoints include mean change heart rhythm at 5 and 15 minutes after administration of diltiazem bolus, mean change heart rate at 5 and 15 minutes after administration of diltiazem bolus, adverse effects due to administration of Calcium gluconate and adverse effects due to administration of Diltiazem infusion.

Full Information

First Posted
December 15, 2022
Last Updated
January 31, 2023
Sponsor
Aurora Health Care
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1. Study Identification

Unique Protocol Identification Number
NCT05661942
Brief Title
Diltiazem in the Treatment of Atrial Fibrillation or Atrial Flutter With Rapid Ventricular Rate
Acronym
AFF RVR
Official Title
Diltiazem in the Treatment of Atrial Fibrillation or Atrial Flutter With Rapid Ventricular Rate (AFF RVR): Comparing Calcium Pre-treatment vs Placebo in Prevention of Diltiazem Induced Hypotension
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 30, 2022 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
June 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aurora Health Care

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To compare the relative efficacy for calcium pre-treatment in decreasing incidence of drug induced hypotension after diltiazem administration for treatment of AFF with RVR. Null Hypothesis: There will be no difference between groups in incidence of hypotension after pretreatment with calcium prior to bolus of diltiazem.
Detailed Description
Non-dihydropyridine calcium channel blockers (CCB) are routinely used in the treatment of atrial fibrillation or flutter with rapid ventricular response (AFF with RVR) however, their use can be limited by drug induced hypotension. This drug induced hypotension limits and complicates CCB use in the treatment of AFF with RVR. Calcium pre-treatment with calcium channel blocker administration has been studied extensively with verapamil administration in preventing drug induced hypotension however, similar studies evaluating calcium pretreatment with diltiazem administration in the prevention of drug induced hypotension are limited. The purpose of our study is to compare the relative efficacy and safety for calcium pretreatment with diltiazem in the treatment of AFF with RVR in preventing drug induced hypotension. This prospective, randomized double-blinded study will evaluate patients who present to the emergency department at Advocate Christ Medical Center (ACMC) with a diagnosis of AFF RVR with ventricular rate greater than or equal to 120 bpm from IRB approval to June 1, 2024. Via simple randomization, patients will be administered Calcium pre-treatment vs control prior to diltiazem administration. Calcium gluconate 1gm or 100 mL of normal saline will be administered as an intravenous infusion over 5 minutes followed by bolus diltiazem 0.25 mg/kg IV push (with a 20mg max) with repeat diltiazem bolus dose after 15 minutes if rate control not achieved 0.35mg/kg IV push. Calcium gluconate will not be administered with repeat doses of diltiazem. Weight-based dosing of diltiazem was most utilized, though some providers may elect to modify based on the clinical scenario. The primary outcome will be the mean difference in systolic blood pressure (SBP) evaluated at 5 and 15 minutes after administration of diltiazem bolus. Secondary outcomes include decrease in heart rate, conversion to sinus rhythm, and adverse effects of medication administered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
AFF With RVR, Atrial Fibrillation With Rapid Ventricular Response (Disorder), Hypotension Drug-Induced
Keywords
diltiazem, calcium

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
92 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Calcium pre-treatment
Arm Type
Active Comparator
Arm Description
Calcium gluconate 1 gram/100ml 0.9% NaCl or 100ml 0.9% NaCl
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
diluent (NS) vials
Intervention Type
Drug
Intervention Name(s)
Calcium pre-treatment
Intervention Description
The intervention is Calcium gluconate 1 gram/100ml 0.9% NaCl or 100ml 0.9% NaCl) over 5 minutes.
Intervention Type
Other
Intervention Name(s)
No Intervention
Other Intervention Name(s)
Placebo
Intervention Description
Placebo/ no calcium pre-treatment.
Primary Outcome Measure Information:
Title
Mean Difference in SBP
Description
The primary endpoint is the Mean difference in SBP evaluated at 5 and 15 minutes after administration of diltiazem bolus. Monitors were set to obtain an automated full set of vitals every 5 minutes after administration of diltiazem.
Time Frame
5 and 15 mins
Secondary Outcome Measure Information:
Title
Mean change in heart rhythm
Description
Secondary endpoints include mean change heart rhythm at 5 and 15 minutes after administration of diltiazem bolus, mean change heart rate at 5 and 15 minutes after administration of diltiazem bolus, adverse effects due to administration of Calcium gluconate and adverse effects due to administration of Diltiazem infusion.
Time Frame
5 and 15 mins

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years or older Able to provide informed consent Primary diagnosis AFF with RVR greater than or equal to 120 bpm Exclusion Criteria: Pregnancy defined as a positive urine HCG Hemodynamically unstable patients (SBP <90, MAP <65) Stated history of systolic heart failure with reduced ejection fraction (<40%) or evidence of acute heart failure or reduced EF (peripheral edema, JVD, pulmonary edema) on clinical exam or bedside echo Patients with left ventricular assist device Sinus node dysfunction or preexcitation with accessory pathway (known diagnosis of SVT, WPW or sick sinus syndrome. Delta waves or other evidence of accessory pathway on EKG) 2nd or 3rd degree atrioventricular block Allergy or sensitivity to any study drugs Previously enrolled in this trial during a different patient encounter Non-English speaking
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael V Cirone, MD
Phone
708-684-5354
Email
michael.cirone@aah.rog
First Name & Middle Initial & Last Name or Official Title & Degree
Dharati Desai, PharmD
Phone
7733568241
Email
dharati.desai@aah.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael V Cirone, MD
Organizational Affiliation
Advocate Aurora Health (AAH)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Advocate Christ Medical Center Emergency Department (ACMC ED)
City
Oak Lawn
State/Province
Illinois
ZIP/Postal Code
60453
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael V Cirone, MD
Phone
708-684-5354
Email
michael.cirone@aah.org
First Name & Middle Initial & Last Name & Degree
Dharati Desai, PharmD
Email
dharati.desai@aah.org
First Name & Middle Initial & Last Name & Degree
Dharati Desai, PharmD

12. IPD Sharing Statement

Plan to Share IPD
No

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Diltiazem in the Treatment of Atrial Fibrillation or Atrial Flutter With Rapid Ventricular Rate

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