Skip to content

HRS study of pacemaker patients

HRS study of pacemaker patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023844
Enrollment
Unknown
Registered
2019-06-14
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-06-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronotropic dysfunction

Interventions

DDDR:Pace mode DDDR

Sponsors

Nanjing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patient is eligible for a dual chamber pacemaker according to current clinical guidelines; 2. Patient is willing and capable of providing informed consent to participate in the study; 3. Patient aged 18 years or above.

Exclusion criteria

Exclusion criteria: 1. Patient has an ICD or CRT device; 2. Patient is currently enrolled in another study that would directly interfere with the current study; 3. Patient is a woman of childbearing potential who is or plans on becoming pregnant during the duration of the study.

Design outcomes

Primary

MeasureTime frame
HRS;Atrial fibrillation load;

Countries

China

Contacts

Public ContactZuoying Hu

Nanjing First Hospital

huzuoying@aliyun.com+86 13951024682

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026