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Physiotherapy treatment for lateral elbow pain.

comparison between blood flow restriction training and mulligan mobilization with movement in the management of lateral epicondylitis - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078610
Enrollment
61
Registered
2024-12-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: M771- Lateral epicondylitis

Interventions

Intervention1: Blood flow restriction training: During exercise, functioning muscles can be trained to partially restrict arterial inflow and restrict venous outflow by a technique called blood flow r

Sponsors

Vidhi Joshi
Lead Sponsor
Dr Sanjib Kumar Das
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Presence of pain on the lateral epicondyle of the elbow. 2. Tenderness on palpation on the lateral epicondyle. 3. Positive cozens, mills, and maudsley’s test results. 4. Complaints persisting for at least 8 weeks. 5. There is an apparent decline in grip strength in the affected arm. 6. Informed consent form signed by participants.

Exclusion criteria

Exclusion criteria: 1. Participants who had a history of surgery on the affected arm. 2. Participants with other upper extremity conditions (e.g. Carpal tunnel syndrome, rotator cuff pathology, biceps tear) that could interfere with the assessment of grip strength and function. 3. Participants who had received the corticosteroid injection around the affected elbow within the past 3 months. 4. Participants with systemic conditions, that may affect the healing or muscle performance (e.g. diabetes, rheumatoid arthritis, chronic inflammatory conditions, and hypertension both controlled and uncontrolled). 5. Participants on blood thinners or anticoagulant therapy, as BFR training could increase the risk of complications. 6. Pregnant women will be excluded due to potential risks associated with BFR training. 7. Participants who will experience significant discomfort, pain, or any other adverse reactions during a trial session of BFR training. 8. Participants with mental or cognitive impairments that could prevent them from understanding the study procedure or following the exercise protocol.

Design outcomes

Primary

MeasureTime frame
Grip strength measurement, Pain intensity, and functional disabilityTimepoint: Baseline, 4th and 6th weeks

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Sanjib Kumar Das

Amity Institute of Health Allied Sciences

skdas@amity.edu8879485847

Outcome results

None listed

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