CIED Post-OR Rehabilitation

Starting soon · Not applicable

Conditions studied: CIED Postoperative Upper Limb Stiffness and Disability

In brief

The purpose of this study is to develop a systematic rehabilitation exercise program (rehabilitation exercise routine), focusing on the rehabilitation training of the upper limb on the implantation side after transvenous cardiac implantable electronic devices (CIEDs) implantation, and to explore its impact on the joint function of the implanted upper limb and the overall quality of life of patients. This study will conduct long-term follow-up by comprehensively using imaging examinations and relevant professional assessment scales, focusing on evaluating the clinical safety of this rehabilitation exercise routine, and simultaneously clarifying its improvement effect on discomfort symptoms (such as pain, stiffness, etc.) and functional abnormalities of the implanted limb, so as to provide scientific basis and practical guidance for the standardized rehabilitation of patients after transvenous CIEDs implantation.

Key facts

Study ID

NCT07494825

Run by

Shanghai Zhongshan Hospital

People needed

600

Starts

2026-04-01

Expected to finish

2026-12-31

Last updated by the study team

2026-03-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients who meet the indications for transvenous CIEDs implantation in accordance with ACC/AHA/HRS or ESC guidelines, including single-chamber, dual-chamber, and triple-chamber pacemakers;
• Patients who have previously implanted a transvenous pacemaker and plan to upgrade the pacemaker requiring the addition of electrode leads;
• Patients aged > 18 years at the time of enrollment;
• The subject (or the patient's legal authorized representative) is willing and able to sign their name and date on the patient informed consent form.

You may not qualify if…

• Subjects aged ≤ 18 years old, pregnant women or lactating patients;
• Patients with disease conditions that the researcher deems inappropriate for participation in this study;
• Patients who have previously implanted a transvenous pacemaker and only need to replace the pulse generator;
• Patients who are simultaneously participating in other clinical studies related to cardiac electronic implantable devices.

Full record on ClinicalTrials.gov

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