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CompletedNCT03071952Updated Jan 11, 2018

Assessment of AAIR Pacing Treatment for Heart Failure Patients With Chronotropic Incompetence

An observational study in Heart Failure, sponsored by Medtronic Cardiac Rhythm and Heart Failure. Completed at 1 site in China. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2018-01-11.

Sponsored by Medtronic Cardiac Rhythm and Heart Failure · Observational

Study type
Observational
Model
Case-crossover
Time perspective
Prospective
Enrollment
11
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The primary objective of this study is to assess the clinical efficacy of AAIR (Atrial-paced Atrial-sensed Inhibitory Rate-Modulated) pacing treatment for heart failure (HF) patients with chronotropic incompetence (CI) in terms of exercise tolerance and quality of life. Specifically, the study will assess the changes in cardiac function associated with changes of physical exercise intensity and heart rate in AAIR pacing mode compared with AAI pacing mode.

Read the detailed description

CI is the inability of the heart to increase its rate in response to increased physical activity or metabolic demand, leading to exercise intolerance and poor quality of life. Studies have demonstrated that patients with CI have a high risk of cardiac morbidity and mortality. Recent studies further demonstrate a high incidence of CI in patients with heart failure, which is also confirmed by CI in Heart Failure Study Phase I. However, clinical attention is often paid to heart failure symptoms instead CI-related symptom. Thus, patients with heart failure are often not tested for CI, even though the CI incidence is high in these patients. Moreover, such patients could gain significant improvements in exercise tolerance and quality of life once they get diagnosed followed by effective therapy for CI and long-term management.

This study is designed to establish clinical evidence that AAIR pacing is beneficial to treat CI-caused symptoms in heart failure patients, which will improve the life quality of such patients and further support the expansion of Brady therapy indications to the population of HF with CI in existing markets and also potential markets.

CI is rarely seen and has different definition among various animal species. It is impossible to use animals to get wanted data for AAIR pacing treatment to CI. Thus, a human clinical study is necessary. Furthermore, exercise testings, such as 6 minutes hall walk (6MHW) and treadmill, allow objective evaluation of exercise capacity and exertional symptoms, which have been suggested as other investigations for HF in "ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012". Therefore, exercise testings will be applied upon physicians' need or judgment.

Firstly, this study is to assess the effect of AAIR pacing treatment for HF patients with CI in terms of exercise tolerance and quality of life. Specifically, the study will assess the changes in cardiac function associated with changes of physical exercise intensity and heart rate in AAIR pacing mode compared with AAI pacing mode. Secondly, the study will look at clinical outcomes in terms of NYHA class, 6MHW, blood BNP, Echo measurements following pacemaker therapy for 1 year. 6MHW and treadmill tests have been suggested as other investigations for HF in "ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012" and will be performed upon physicians' need or judgment.

The study will enroll up to 30 subjects that meet the indication for pacing therapy. Consented subjects will receive pacing therapy and two follow-ups in the following one year.

02

Conditions studied

  • Heart Failure

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Keywords

  • Heart Failure
  • Chronotropic Incompetence
  • Rate Response
  • Exercise Test
03

In context

Heart Failure

5,701 studies on the registry are indexed under Heart Failure; 1,220 are open to participants now.

This study's enrollment of 11 is below the median of 200 across 1,679 observational studies indexed under Heart Failure.

Browse Heart Failure studies →

Lead sponsor

Medtronic Cardiac Rhythm and Heart Failure is the lead sponsor of 239 studies on the registry; 6 are open to participants now.

Of its 19 completed or terminated interventional studies of FDA-regulated products, 17 (89%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

In the study, total 30 heart failure patients with chronotropic incompetence who meet the inclusion and exclusion criteria would be enrolled from the ourtpatients in Fuwai Hospital.

Inclusion criteria

  • Patient is willing to give informed consent.
  • Patient is between 18 and 70 years of age (including 18 and 70 years of age).
  • Patients can perform treadmill exercise test for at least 8 minutes.
  • Patient has been diagnosed with stable chronic HF according to HF guidance, including HFpEF (Heart Failure with preserved Ejection Fraction) and HFrEF (Heart Failure with reduced Ejection Fraction) patients.
  • NYHA class I- III, with left ventricular ejection fraction less than 55% and more than 25%.
  • Heart rate during treadmill test cannot reach 70% APMHR (Age Predicted Maximal Heart Rate) in (diagnostic criteria for CI, in accordance with class IA indications of pacing therapy for CI).

Exclusion criteria

Exclusion Criteria:

  • Patient with severe liver or kidney dysfunction.
  • Patient has contraindications for pacing therapy.
  • Patient has CI and is under appropriate clinical therapy.
  • Patient has persistent or permanent atrial fibrillation (AF).
  • Patient whose heart rate baseline at resting state is greater than 95 beats per minutes (BPM).
  • Patient has contraindications for cardio-pulmonary exercise testing, including but not limited to unstable angina, decompensated heart failure, active pericarditis or myocarditis, hypertrophic cardiomyopathy, valvular heart disease and ECG ST-segment shift > 2mm at resting state.
  • Less than 6 months after angina and ST dynamic changes during last 3 months.
  • Patient with class I (with PR interval more than 200ms), II or III atrioventricular block, or interventricular block.
  • NYHA Class IV.
  • Less than 45 days after myocardial infarction.
  • Less than 3 months after acute heart failure.
  • Patient has uncontrolled hypertension.
  • Patient is unwilling to sign the patient informed consent.
  • Patient is pregnant or has pregnancy intention in the study duration.
  • Patient has a medical condition that would limit study participation.
  • Patient is enrolled in a concurrent study that may affect the outcome of this study.
05

Study design

Observational model
Case-crossover
Time perspective
Prospective
Enrollment
11 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. The treadmill walk duration change

    Time frame: The treadmill walk duration change from 3-6 months to 6-12 months post pacemaker implantation

Secondary outcomes

  1. The 6 minutes hall walk distance change

    Time frame: 3-6 months and 6-12 months post pacemaker implantation

07

Study locations

1 site
  • Fuwai Hospital
    Beijing, Beijing 100037, China
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 11, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03071952
Lead sponsor
Medtronic Cardiac Rhythm and Heart Failure
Responsible party
Sponsor
First posted
Mar 7, 2017
Start date
Oct 9, 2016
Primary completion
Nov 24, 2017
Completion
Nov 24, 2017
Last update
Jan 11, 2018

Study contacts

Shu Zhang, PhD
principal investigator · Chinese Academy of Medical Sciences, Fuwai Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2018. You cannot join it, but the record below documents what was studied.

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