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Iontophoresis & Knee Osteoarthritis in elderly

FORMULATION AND EFFICACY OF A NEW IONTOPHORETIC GEL ON PAIN FUNCTION QUALITY OF SLEEP AND WALKING PATTERNS OF SPEED OSTEOARTHRITIC PATIENTS AN EXPERIMENTAL STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043155
Enrollment
115
Registered
2022-06-10
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: An iontophoretic gel: Each patient will be asked to lie in supine position. Once comfortable, maximum painful area will be located and marked on the affected knee. The active electrode

Sponsors

PARUL SHARMA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 male and female aged between 40 and 60 years 2 Patients with unilateral knee osteoarthritis of grade I-II on Kellgren and Lawrence (K-L) radiological ( X-Ray) classification 3 Subjects with pain 4-7 on a numerical pain rating scale will be included

Exclusion criteria

Exclusion criteria: 1 Subjects with any traumatic, metabolic, infective, or rheumatic condition affecting the knee joint. 2 Subjects with pain referred from proximal joints like the hip joint, sacroiliac joint, or lumbar spine. 3 Subjects contra-indicated for treatment with laser therapy/ iontophoresis. 4 Patients who had severe OA (grade IV according to the Kellgrenâ??Lawrence system of classification). 5 Poorly controlled diabetes mellitus with fasting blood sugar greater than 11.1 mmol/L. 6 History of anticoagulation therapy. 7 History of prior total knee replacement surgery. 8 Any dermatological problems

Design outcomes

Primary

MeasureTime frame
â?¢Knee ROM in flexion will be determined in prone position using a Goniometer. Pain intensity will be assessed by Visual analog scale â?¢Pain will be measured using a 10 cm VAS. â?¢The WOMAC questionnaire is used to evaluate a patientâ??s functions when diagnosed with rheumatic diseases, especially knee OA. â?¢The Medical Outcome System (MOS) sleep scale will be used to take assessment of sleep at the beginning and end of the study Timepoint: baseline immediately following intervention

Secondary

MeasureTime frame
WOMAC QUESTIONNAIRE Medical outcome system sleep scale Timepoint: Baseline Immediately following intervention

Countries

India

Contacts

Public ContactMANOJ MALIK

Delhi Pharmaceutical Sciences and Research University

tonkrk@dpsru.edu.in8851229156

Outcome results

None listed

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