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Evaluation of effectiveness of IndoKnee during knee flexion and extension

A non-randomized single arm trial to evaluate the effectiveness of IndoKnee during Knee flexion and extension.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/07/020059
Enrollment
30
Registered
2019-07-05
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: IndoKnee (A device for knee support): Use IndoKnee (A device for knee support) for 2-4 weeks, perform tasks involving knee flexion and extension. Control Intervention1: Without IndoKnee

Sponsors

Newndra Innovations Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Healthy Male and Female subjects. Age should be between 18 years to 70 years Height should be between 145cm to 180cm Normal Healthy Person (BMI should be between18 to 30).

Exclusion criteria

Exclusion criteria: Cases of known or suspected knee injury, Knee replacement, Knee surgery Subjects underwent surgery or advised not to squat Pregnant women

Design outcomes

Primary

MeasureTime frame
Evaluate the effectiveness of using IndoKnee during knee flexion and extension by assessing the EMG data Analysis of EMG data shows the effectiveness or non-effectiveness of using IndoKnee Timepoint: 1 Year—

Secondary

MeasureTime frame
To assess the ease of use, risks and adverse effects and get feedback for the device, understand the gap between device and user requirements.Timepoint: 1 Year—

Countries

India

Contacts

Public ContactDr Anil Kumar Jain

Santokba Durlabhji Memorial Hospital cum Medical Research Institute

pksrc@sdmh.in9829061496

Outcome results

None listed

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