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Effectiveness of Buerger- Allen exercise

A study on effectiveness of Buerger- Allen exercise in improving circulation and cardiovascular fitness in coronary artery bypass graft (CABG) patients?with?diabetes - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/093961
Enrollment
26
Registered
2025-09-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: I703- Atherosclerosis of unspecified type of bypass graft(s) of the extremities

Interventions

Intervention1: Routine care: General physio care Intervention2: Routine Care: General Physio Care One person it takes around 2 weeks period Control Intervention1: Buerger-Allen exercise with Routine

Sponsors

Bhoomika D
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with type2 diabetes mellitus who undergone CABG post operative (after 1 week) and medically stable, Patients with mild to moderate peripheral arterial insufficiency(ABI-0.5-0.9), Patients who are stable to perform buerger-Allen exercises, Patients with stable vital signs, Patients who are willing to participate

Exclusion criteria

Exclusion criteria: Severe Peripheral Arterial Disease Patients with lower ABI lesser than 0.5(indicating critical limb ischemia),Diabetic neuropathy (with loss of protective sensation), Uncontrolled diabetes HbA1c greater than 10 percentage, Unstable Cardiovascular Condition ? Ejection fraction less than 50 percentage, Heart failure, Severe Postoperative complications (DVT, Excessive bleeding), Unstable hemodynamic(requiring inotropic support), CABG with three vessel diseases , Other musculoskeletal, Neurological disorders, Psychiatric disorders, Other Medical Conditions Affecting Participation Chronic kidney disease stage 4 or 5 (on dialysis), Severe respiratory disease (with oxygen dependency), Any active infection or fever, Refusal to Participate -Patients who do not provide informed consent or are unwilling to follow the exercise regime

Design outcomes

Primary

MeasureTime frame
1.Ankle Brachial Index 2.Modified Harvard Step Up TestTimepoint: 6 Months

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactC H Anand Chellappa

College Of Physiotherapy, Sri Ramakrishna Institute Of Paramedical Science

anandreena2016@gmail.com9629733374

Outcome results

None listed

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