CClinicalTrials.gg
Active, not recruitingNCT04148703TELEPACEUpdated Jun 6, 2023

Cost-utility Analysis of the Follow-up of Exclusive Telemedicine Pacemakers, Compared to Conventional Pacemakers

An interventional study of Follow up post Pacemaker implantation in office and Follow up post Pacemaker implantation by home monitoring in Single or Dual Chamber Pacemaker Implantation and Home Monitoring Follow-up, sponsored by Nantes University Hospital. Active, not recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-06-06.

Sponsored by Nantes University Hospital · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by May 2025, 1 year 5 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
620
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

TELEPACE is an economic evaluation that aims to determine the probability at which Home Monitoring without physical examinations, could be cost effective, compared to the conventional treatment by face to face consultations. Patient will be randomized in a control group followed according to the current guidelines and and active group exclusively followed by remote monitoring. The study will end after a 4 year follow-up.

Read the detailed description

Professional practice guidelines recommend that pacemakers be followed with at least one to two in-office follow-ups per year, which is both a public health issue (the average time to get a consultation with a cardiologist being 42 days) but also an economic issue considering the number of patients implanted (Brignole EHJ 2013). Remote monitoring of pacemakers could allow an optimization of the long-term follow-up of pacemaker recipients in hospitals.

Compared to CRT and ICD, few studies have highlighted the economic advantage of remote monitoring with PM.

COMPAS study (Eur Heart J. 2012) demonstrated that remote monitoring is a safe alternative to conventional care over a 2 year-follow-up. This study also demonstrated that long-term remote monitoring of pacemakers decreased the number of ambulatory visits and enabled the early detection of important clinical and device-related adverse events.

As the study shows data up to 18 months, this is not sufficient to define the benefit of telecardiology in this population of patients.

SETAM study (Pacing Clin Electrophysiol 2017) demonstrated the benefit of remote monitoring showing an earlier diagnosis and management of atrial arrhythmias and a subsequently reduction of atrial fibrillation (AF) burden. The incidence and prevalence of AF is expected to increase with time, resulting in significant societal and economic impact.

Neither COMPAS nor SETAM were designed as economic evaluations

TELEPACE study proposes the first economic evaluation of an exclusive follow-up by Home-Monitoring of patients implanted with pacemaker for a period of 4 years.

All patients will be implanted with a single or dual chamber pacemaker according the implantation guidelines. Patients enrolled will be then randomized to a control group or an active group:

  • The patients randomized in the control group will be followed accordingto the guidelines; i.e. with an in-office follow-up at 30 days post-implantation and after followed with in-office follow-ups according toclinical practice.
  • Active group: in-office follow-up at 30 days post-implantation and after by remote monitoring (daily) without scheduled in-office follow-up during the study period (48 months). A remote FU will be planned every 9 months.

Consequently, compared to the guidelines, the patients in the active group will be followed according to the guidelines; except for the in-office follow-ups annually.

By collecting real costs directly on health insurance reimbursement bases (SNIIRAM), this study will define the medico-economic benefit of remote monitoring of pacemakers.

A cost-utility analysis is needed to address the question. The use of QALYs is not intended to demonstrate a difference in clinical efficacy but to ensure that efficacy and costs are studied simultaneously which is required in order to avoid risk inflation when differences in efficacy and costs are studied sequentially.

If there is no significant differences in QALYs (as expected) but there are savings in terms of HSR then the cost-utility ratio will allow to estimate a "net benefit criterion" (NBC) that translates QALYs into money as follows: NBC = WTP.(differences in QALYs) - (differences in costs) where WTP represents the (societal) willingness to pay a QALY.

If there is no differences in QALYs the NBC will then reduce to a cost-minimisation calculus (WTP.(diff QALYs) = 0).

Cost-minimisation alone can only be used (HAS regards it as a sub-category of cost-effectiveness analysis whose use has to be duly justified) provided that there is strong evidence of equivalence in terms of clinical efficacy. If this is not the case, a cost-utility analysis will be more relevant as it will test simultaneously for both differences in efficacy and in costs.

Moreover, the study will confrim the safety of telecardiology and evaluate patients' individual preferences for the different management strategies.

02

Conditions studied

  • Single or Dual Chamber Pacemaker Implantation
  • Home Monitoring Follow-up

Keywords

  • Pacemaker, home monitoring, remote monitoring, ecocomic
03

In context

Lead sponsor

Nantes University Hospital is the lead sponsor of 825 studies on the registry; 195 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Single or dual chamber pacemaker implantation patients
  • patients agree to be enrolled in the study and followed during 4 years
  • patients have insurance coverage

Exclusion criteria

Exclusion Criteria:

  • Minor patients
  • personn with disability
  • pregnant women
  • patient with life expectancy of less than 4 years
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
620 participants (actual)

Study arms

  • Experimental
    Active group

    in-office follow-up at 30 days post-implantation and after by remote monitoring (daily) without scheduled in-office follow-up during the study period (48 months). A remote FU will be planned every 9 months.

    Other: Follow up post Pacemaker implantation by home monitoring

  • Active comparator
    Control group

    The patients randomized in the control group will be followed accordingto the guidelines; i.e. with an in-office follow-up at 30 days post-implantation and after followed with in-office follow-ups according to clinical practice.

    Other: Follow up post Pacemaker implantation in office

Interventions

  • OtherFollow up post Pacemaker implantation in office

    All patients will be implanted with a single or dual chamber pacemaker according the implantation guidelines and will be followed by in-office follow-up

  • OtherFollow up post Pacemaker implantation by home monitoring

    All patients will be implanted with a single or dual chamber pacemaker according the implantation guidelines and will be followed by home monitoring

06

What researchers measure

Primary outcomes

  1. ICER (incremental cost effectivness ratio)

    cost and medical consumtion collected with the French insurance care database

    Time frame: 4 years

  2. QALY

    Quality Adjusted Life Years estimated by EQ5D-5L

    Time frame: 4 years

Secondary outcomes

  1. Safety of home monitoring

    time limit compensation claim (delay between the diagnosis and the therapy)

    Time frame: 4 years

  2. Safety of home monitoring

    combined criteria (death, stroke, heart failure, arrhythmia, pacemeker dysfunction, infection, hospitalization)

    Time frame: 4 years

07

Study locations

1 site
  • GOURAUD Jean-Baptiste
    Nantes, 44000, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04148703
Lead sponsor
Nantes University Hospital
Collaborators
Tours University Hospital, University Hospital, Marseille, Rennes University Hospital, Toulouse University Hospital, University Hospital, Clermont-Ferrand, Angers University Hospital, Lille University Hospital, University Hospital, Strasbourg, France, University Hospital, Rouen, Montpellier University Hospital, University Hospital, Brest, Pau University Hospital
Responsible party
Sponsor
First posted
Nov 1, 2019
Start date
Nov 4, 2019
Primary completion
May 5, 2025 (estimated)
Completion
May 5, 2025 (estimated)
Last update
Jun 6, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in May 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion