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Efficacy of Vatagajankusha Rasa over Ekangaveera Rasa after virechana in the management of Pakshaghata (Hemiplegia)

Evaluation of the effect of Vatagajankusha Rasa over Ekangaveera Rasa after virechana in the management of Pakshaghata (Hemiplegia): A Randomised Controlled Clinical Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/10/096458
Enrollment
30
Registered
2025-10-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

None listed

Sponsors

All India Institute Of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients with the signs and symptoms of Pakshaghata (Hemiplegia). 2) Chronicity, up to 3 years. 3) NIHSS score up to 16 4) Ischemic stroke. 5) Subjects aged 21-60 years. 6) Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study. 7) Subjects who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, and other study procedures.

Exclusion criteria

Exclusion criteria: 1) Does not sign informed consent or refuses to cooperate with treatment. 2) Patients not meeting the diagnostic criteria 3) Diagnosed cases of intracranial hemorrhage, intracranial space-occupying lesion, Congenital defects, carcinoma, basal ganglia infarct, and intracranial infections. Comatose and unconscious patients. 4) Hemorrhagic stroke 5) Pregnant women, lactating mothers. 6) Systemic illness uncontrolled HTN (More than 160/90 mmHg), CKD, uncontrolled T2DM (HbA1C greater than 8 %)

Design outcomes

Primary

MeasureTime frame
A change in NIH Stroke Scale . Improvement the clinical signs and symptoms of Pakshaghata – Hataeka paksha, Cheshta nivriti, ruja, vakstambha, sira-sanayu vishosha Timepoint: Baseline After 57 days After 85 days

Secondary

MeasureTime frame
1 Changes in the modified Rankin Scale (mRS) . 2 Changes in the Modified Ashworth Scale (MAS). 3 Improvement in quality of life of the patient. Timepoint: Baseline After 57 days After 85 days

Countries

India

Contacts

Public ContactDr Aditi Sharma

All India Institute Of Ayurveda

jonahdr@gmail.com8589805246

Outcome results

None listed

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