Effect of multidimensional ayurvedic treatment in people with one-sided paralysis: a single group before and after clinical study

Effect of multidimensional ayurvedic management of pakshaghata: a single-group pre- and post-design clinical study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/101931

Enrollment

Registered

2026-01-23

Start date

Unknown

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Health Condition 1: G819- Hemiplegia, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed clinically as pakshaghat (Hemiplegia) based on ayurvedic and modern diagnostic parameters. Patients between age group of 18 to 70 years of both genders. Patients who are clinically stable post-stroke and, in a condition, to receive therapy. Patients with stroke onset not older than 5 years (i.e., subacute to moderately chronic stage).

Exclusion criteria

Exclusion criteria: Patient with severe systemic illness (e.g., Cardiac Failure, Chronic Renal Disease, Hepatic Failure, Malignancy). Patient with Uncontrolled Hypertension (greater than 160 by 100mmHg - stage II - JVC 7 classification), Uncontrolled blood sugar (PPBS - greater than 250 mg per dL). Patients with recurrent or multiple strokes or other neurodegenerative disorders (e.g., MND, Parkinsonism). Patients contraindicated for virechan, basti, nasya, or other procedures planned in the protocol. Patients with psychiatric illness or cognitive dysfunction that may interfere with study compliance. Patients with infective conditions, metabolic disorders, bleeding disorders, or any other emergency medical conditions.

Design outcomes

Primary

Measure	Time frame
To assess the impact of multidimensional management on the clinical signs and symptoms of pakshaghat.Timepoint: Baseline (pre-treatment), After completion of the IPD treatment, During the follow-up period at 2-week intervals, up to 8 weeks post-discharge.	—

Secondary

Measure	Time frame
To evaluate the improvement in motor and sensory functions using standard clinical and functional assessment tools.Timepoint: Baseline (pre-treatment), After completion of the IPD treatment, During the follow-up period at 2-week intervals, up to 8 weeks post-discharge.	—

Countries

India

Contacts

Public ContactDr Vishnu V Nath

J S Ayurveda Mahavidhyalaya and P D Patel Ayurveda Hospital

ayur.vishnuvijayanath@gmail.com9481136020

Outcome results