Trial Outcomes & Findings for Catheter Ablation of Arrhythmias to Improve CRT Response (NCT NCT03035227)

NCT ID: NCT03035227

Last Updated: 2022-09-10

Results Overview

Change in Ejection Fraction (EF)

Recruitment status

TERMINATED

Study phase

PHASE4

Target enrollment

2 participants

Primary outcome timeframe

90 Days

Results posted on

2022-09-10

Participant Flow

Participant milestones

Participant milestones
Measure
Medical Therapy
The medical treatment arm consist of the use of antiarrhythmic drugs that are deemed to be appropriate for the given arrhythmia by the treating physician.
Ablation Arm
Patients enrolled into the ablation arm will under go catheter ablation of atrial or ventricular arrhythmia within 3 months of signing the informed consent form.
Overall Study
STARTED
1
1
Overall Study
COMPLETED
0
0
Overall Study
NOT COMPLETED
1
1

Reasons for withdrawal

Reasons for withdrawal
Measure
Medical Therapy
The medical treatment arm consist of the use of antiarrhythmic drugs that are deemed to be appropriate for the given arrhythmia by the treating physician.
Ablation Arm
Patients enrolled into the ablation arm will under go catheter ablation of atrial or ventricular arrhythmia within 3 months of signing the informed consent form.
Overall Study
study stopped due to PI leaving institut
1
1

Baseline Characteristics

Catheter Ablation of Arrhythmias to Improve CRT Response

Baseline characteristics by cohort

Baseline data not reported

PRIMARY outcome

Timeframe: 90 Days

Population: data not analyzed

Change in Ejection Fraction (EF)

Outcome measures

Outcome data not reported

PRIMARY outcome

Timeframe: 90 Days

Population: data not analyzed

data not analyzed

Outcome measures

Outcome data not reported

PRIMARY outcome

Timeframe: 365Days

Population: data not analyzed

data not analyzed

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 365 Days

Population: data not analyzed

data was not analyzed

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 365 Days

Population: data not analyzed

data not analyzed

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 30 Days

Population: data not analyzed

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 30 Days

Population: data not analyzed

data not analyzed

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 30 Days

Population: data not analyzed

data not analyzed

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 30 Days

Population: data not analyzed

data not analyzed

Outcome measures

Outcome data not reported

Adverse Events

Medical Therapy

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Ablation Arm

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr. Dhanunjaya Lakkireddy

Kansas City Heart Rhythm Institute

Phone: 913-449-1297

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place