"DESIGNING AND TESTING COMPRESSON VIBRATORY COMBINATION DEVICE FOR LOWER LEG LYMPHATIC EDEMA"

"DESIGNING AND TESTING COMPRESSON VIBRATORY COMBINATION DEVICE FOR LOWER LIMB LYMPHEDEMA: AN EXPLORATIVE STUDY"

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/01/049083

Enrollment

Registered

2023-01-18

Start date

Unknown

Completion date

Unknown

Last updated

2023-02-06

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

Conditions

Health Condition 1: I89- Other noninfective disorders of lymphatic vessels and lymph nodes

Interventions

Intervention1: Compression Vibratory Combination Device: Treatment Time Will be 45 minutes for pneumatic compression and 15 minutes for vibration therapy, 5 days/week for 3 months Control Intervention

Eligibility

Inclusion criteria

Inclusion criteria: All grades of lymphedema Lower limb lymphedema diagnosed by registered medical officer

Exclusion criteria

Exclusion criteria: Non co-operative patients Mental retarded patients Do not come for follow up Patient with Cellulitis and local skin infection Cardiac condition(congestive heart failure) Arterial occlusion disease Deep vein thrombosis Unhealed fracture Loss of sensation

Design outcomes

Primary

Measure	Time frame
Girth MeasurementTimepoint: Baseline	—

Secondary

Measure	Time frame
NILLTimepoint: NILL	—

Countries

India

Contacts

Public ContactDenisha Radadia

School Of Physiotherapy, RK University

nidhi.ved@rku.ac.in9408004454

Outcome results

None listed

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