NCT04331249Recruiting
Perioperative Management Evaluation in Patients With CIED
Perioperative Management Evaluation in Patients With Implanted Cardiac Electronic Devices
Source: ClinicalTrials.gov · Last updated 15 Oct 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Background: Recommendations for peri-operative management in patients with implanted cardiac electronic devices (CIED) are often based on older data from case reports and small collectives. Objective: To evaluate the peri-operative management and outcome of patients with implanted CIED undergoing non-CIED related surgery or catheter-interventional procedures in clinical routine. Study design: bi-center, non-randomized, observational registry, retrospective data-collection, on-going prospective patient enrollment, descriptive statistics Primary endpoint: number and type of peri-operative adverse device related events (ADE) Secondary endpoints: pre-interventional data (patient characteristics, data from CIED interrogation); peri-interventional data (type of surgery/intervention, anesthesiology techniques, any AE), postinterventional data (data from post-interventional CIED interrogation, need for reprogramming / device revision). Inclusion criteria: implanted CIED, non-CIED related surgical or catheter-based intervention, peri-procedural CIED interrogation, age \>18 years Exclusion criteria: no implanted CIED, no data from any peri-procedural CIED interrogation available Patient enrollment: retrospectively beginning from 2008, further on-going prospective inclusion Sample size: For the observational study, there is no pre-specified sample size. Data from more than 500 patients undergoing \> 700 interventions are expected.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 500 (estimated)
- First submitted
- 31 Mar 2020
- Start date
- 27 Nov 2018
- Primary completion date
- 31 Dec 2025
- Lead sponsor
- Klinikum-Fuerth
- NCT number
- NCT04331249
What you commit to
- Study type: Observational
- Planned participants: 500
- From 27 Nov 2018 to the primary completion date, 31 Dec 2025
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- no implanted CIED,
- no data from any peri-interventional CIED interrogation available
Who the study is looking for
- implanted CIED (e.g. pacemaker, ICD, CRT),
- performed (non-CIED related) surgical or catheter-based procedure,
- data from peri-procedural CIED interrogation available
- age \>18 years
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Klinikum Fuerth Coordinator of this site? Confirm its status | Fürth | Germany | Recruiting |
| Klinikum Nuernberg Coordinator of this site? Confirm its status | Nuremberg | Germany | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.