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Development of artificial hand for paralyzed patients

Development of wearable artificial muscle for a Tetraplegic Hand

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019054
Enrollment
20
Registered
2019-05-10
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

Health Condition 1: G952- Other and unspecified cord compression

Interventions

Intervention1: Chronic cervical spinal cord injured patients with upper limb paralysis: The patients will be given routine physiotherapy along with the artificial hand being developed. The scores will

Sponsors

Canad India SCI Innovation award
Lead Sponsor
IC IMPACTs RHI ISIC
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Cervical spinal cord injured individuals, 18 years of age or older , ASIA A, B, C Have sustained a SCI for the preceding 6 months, Ability to hold a 2.54-cm block of Box and Block apparatus with the thumb

Exclusion criteria

Exclusion criteria: Any co-morbidities with SCI such as head injury or any other injury affecting the the target hand (e.g. brachial plexus or peripheral nerve injuries) have had trauma or surgery to the target hand or upper limb within the last 12 months amputation of any digits on the target hand not able to sit out of bed for at least two hours per day over three consecutive days Any psychiatric illness diagnosed Unstable patients Contractures in targeted hand, spasticity more than grade 1 on modified ashworth scale

Design outcomes

Secondary

MeasureTime frame
A soft robotic glove for hand functionality augmentation for tetraplegic patient. Initial functionality, based on what the control system would be developed is a grasping movement. In short, a wearable gloves, which will act as an external muscle, and help the patient fold his hand to grasp.Timepoint: The assessment will be done at 0,3 and 6 months period after the gloves are made. THe neurology and outcome measures will be compared.

Primary

MeasureTime frame
A soft robotic glove for hand functionality augmentation for tetraplegic patient. Initial functionality, based on what the control system would be developed is a grasping movement. In short, a wearable gloves, which will act as an external muscle, and help the patient fold his hand to grasp.Timepoint: o, 3 and 6 months assessment will be done using neurlogical scales.

Countries

India

Contacts

Public ContactDr H S Chhabra

Indian Spinal Injuries Centre

drhschhabra@isiconline.org

Outcome results

None listed

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