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Electro-Acupuncture Treatment for knee pain

Clinical Outcome of Electro-Acupuncture in the Management of Knee Bi Syndrome:An Acupuncture And Energy Medicine Based Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099185
Enrollment
100
Registered
2025-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Electroacupuncture: The study group will receive electroacupuncture at six specific TCM acupoints:MEDIAL XIYAN(Medial-eye of the knee),SP5(Shangqiu),SP9(Yinlingquan),ST35(Dubi),ST36(Zus

Sponsors

Dr Dinesh kumar S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients were diagnosed with knee pain (symptoms - pain, swelling,warm,stiffness).2.The participants who have the range of motion (ROM) below 130 .3.Body mass index (BMI)lesser than 35.4.The participants are included under the TCM based knee bi syndrome questionaries (Bothmoderate and severe).

Exclusion criteria

Exclusion criteria: 1.Patients with severe osteoarthritis requiring surgical intervention or history of lower-limbjoint (knee joint) arthroplasty surgery.2.Presence of other diseases causing pain or dysfunction of the lower limb, apart from kneejoint disease. (Lumbar disc herniation, Parkinson s disease, Alzheimer s disease, Neuromuscular disorder, etc.)3.Patients who had undergone any cardiovascular surgery (coronary stent or pacemaker)or epilepsy.4.Patients with Psychiatric conditions such as Schizophrenia or Depression.5.Pregnant or lactating women.6.Patients who are afraid of needles (Trypanophobia) & disorders of coagulopathy(e.g., hemophilia).7.Individuals who are undergoing chemotherapy sessions.8.Participation in another clinical study within the last 30 days.

Design outcomes

Primary

MeasureTime frame
1.Range of Motion (ROM): Assessed using a universal goniometer to measure knee flexion and extension.2.Assessment of TCM Knee Bi Syndrome Assessment Questionnaire (TCM-KBSAQ) before and after the intervention.Timepoint: Baseline, 1st week and 3rd week

Secondary

MeasureTime frame
1.Pain related disability: Will be measured by using the Pain Disability Index(PDI) score.2.Inflammatory marker (ESR): By lab investigation.Timepoint: Baseline,1st week and 3rd week

Countries

India

Contacts

Public ContactDr S Geetanjali

International Institute of Yoga and Naturopathy Medical Sciences

drgeethu.nat007@gmail.com6379377297

Outcome results

None listed

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