RecruitingNot Applicable

Evaluating the Safety and Effectiveness of 5G Cloud Follow-up for Cardiovascular Implantable Electronic Devices

China688 participantsStarted 2024-11-13

Plain-language summary

Objective: This clinical study employs a prospective, paired, self-controlled, non-inferiority, multicenter research design to assess the safety and efficacy of utilizing 5G cloud follow-up for CIED in parameters monitoring and remote programming post-implantation. Participants will: undergo regular clinic follow-up visits in accordance with the guidelines undergo routine in-office follow-up and 5G cloud follow-up during each regular clinic visit

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Age ≥ 18 years, gender unspecified;
✓. Patients who have not undergone their first clinic follow-up after the implantation of cardiovascular implantable electronic devices (CIED); Note: In this study, CIED includes pacemakers, implantable cardioverter defibrillators (ICD), cardiac resynchronization therapy pacemakers (CRT-P) and defibrillators (CRT-D), excluding implantable cardiac event recorders (ICM) and implantable cardiovascular monitors.
✓. Willing to participate in this clinical study and have signed the informed consent form in writing.

Exclusion criteria

✕. Life expectancy \< 1 year.
✕. Inability to cooperate with treatment or follow-up, such as having mental illness.
✕. Participated in other clinical studies within 30 days before enrollment. Other situations that the researcher deems unsuitable for inclusion.

What they're measuring

Parameter Measurement Consistency

Timeframe: through study completion, an average of 1 year

Trial details

NCT IDNCT06652750

SponsorThe Third People's Hospital of Chengdu

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-02-01

Contact for this trial

Lin Cai, master of medicine

8619980510703 clin63@yeah.net

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