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Compare the effect of LIPUS and LICUS on pain and disability among adults in knee osteoarthritis - A Pilot Study

Comparating the efficacy of Low intensity pulsed Ultrasound with Low intensity continuous Ultrasound on pain and disability among adults with Knee osteoarthritis - A Pilot study. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/083932
Enrollment
30
Registered
2025-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M15-M19- Osteoarthritis

Interventions

Sponsors

Zikra Fatima
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Participants should be between 40 and 75 years old. 2.Mild to Moderate Knee osteoarthritis confirmed by x-ray. 3. Moderate to severe pain level on VAS. 4. Must have Knee pain or stiffness for at least 3 months. 5.Ability to understand and comply with study procedures.

Exclusion criteria

Exclusion criteria: 1. Prior Knee surgery 2. Current use of anti-inflammatory medications that could confound results. 3. Presence of skin lesions or infections at the treatment site. 4. Pregnancy or significant comorbidities.

Design outcomes

Primary

MeasureTime frame
VAS (Visual analogue scale) Timepoint: Base line (Day 0, before treatment) day-3 Week-1(Day -7 ) week 2(Day -14) Week -3(Day -21) Week-4 (day 28 Final assessment

Secondary

MeasureTime frame
WOMAC (The Western Ontario and Mc Master Universities osteoarthritis Index)Timepoint: Base line (Day 0, before treatment) week 2 (day 14) week 4( Final assessment day 28)

Countries

India

Contacts

Public ContactZikra Fatima

Galgotias University

shinny00720@gmail.com97797 61606

Outcome results

None listed

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