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Feasibility and safety of early walking after catheter ablation of atrial fibrillation: A randomized, non-inferiority clinical trial

Feasibility and safety of early walking after catheter ablation of atrial fibrillation: A randomized, non-inferiority clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120850
Enrollment
Unknown
Registered
2026-03-20
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

atrial fibrillation

Interventions

test group :Manual compression to stop bleeding + bandage salt bag pressure for 4 hours later, exercise on the ground
control group :Manual compression to stop bleeding + bandage salt bag pressure for 6 hours later, exercise on the ground

Sponsors

The Second Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-80 years old; 2.Patients with atrial fibrillation undergoing catheter ablation; 3.Patients who signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Preoperative Exclusion Criteria: (1) Presence of skin infection or inflammation in the groin area or systemically; (2) Prior history of interventional surgery or catheterization via the femoral artery or vein; (3) Presence of hematological disorders; (4) Long-term use of high-dose systemic corticosteroids; (5) Presence of severe comorbidities or complications. 2.Intraoperative Exclusion Criteria: After obtaining informed consent, patients underwent appropriate radiofrequency ablation. Patients were further excluded from the study if any of the following occurred during the ablation procedure: (1) Attempted ablation via femoral artery access or inadvertent puncture of the femoral artery; (2) Occurrence of severe hemorrhage, thrombosis, or other serious complications during the procedure; (3) Difficulty with needle insertion or catheter sheath placement; (4) Incorrect positioning of the sheath.

Design outcomes

Primary

MeasureTime frame
access site bleeding ;puncture site hematoma ;Lower limb thrombosis ;false aneurysm ;arteriovenous fistula ;

Countries

China

Contacts

Public ContactLiang Bin

The Second Hospital of Shanxi Medical University

tyliangbin@163.com+86 139 9423 5827

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026