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Clinical Trials/NCT02315313
NCT02315313UnknownNot Applicable

The Link Between the Clinical Resting Heart Rate and Sympathetic Overactivation

Ruijin Hospital0 sites1,000 target enrollmentStarted: December 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
1,000
Primary Endpoint
The difference of HRV, BPV, LF/HF between each groups

Study Overview

Brief Summary

It is a retrospective study with no products limitation to investigate the link between clinical resting HR and SOA. Use HR≤60bpm as control group, compare other three groups with the control group and find out the correlation between HR and SOA indexes.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Retrospective

Eligibility Criteria

Ages
20 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Provision of subject informed written or oral consent
  • Female and male aged≥ 20 to ≤ 80 years;
  • Records on mean clinical heart rate and SOA indexes were available.

Exclusion Criteria

  • Participation in another clinical study with an investigational product during the last 6 months;
  • Drug intervention on heart rate 1 month prior to the inclusion;
  • Patients with missing data in the database from the Shanghai Institute of Hypertension, Ruijin Hospital, Shanghai.

Outcomes

Primary Outcomes

The difference of HRV, BPV, LF/HF between each groups

Time Frame: 1min HR measure

The difference on mean sympathetic overactivation related indexes such as HRV, BPV, LF/HF between groups

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Wang Jiguang

Director, The Shanghai Institute of Hypertension

Ruijin Hospital

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