Homoeopathy for recovery of muscle weakness after stroke

Homoeopathy in Management of Post- Stroke Spasticity: A Randomized, Single-Blind Pilot Trial - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/06/089740

Enrollment

Registered

2025-06-27

Start date

Unknown

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Health Condition 1: I699- Sequelae of unspecified cerebrovascular diseases

Interventions

Intervention1: Individualized Homoeopathic Medicine plus Physiotherapy: Individualized homoeopathic medicine will be prescribed as per principle of homoeopathy. Indicated medicine will be prescribed o

Eligibility

Inclusion criteria

Inclusion criteria: Any gender aged between 18 years and 80 years. All stroke patient after 1 month post stroke. Stroke patients under Stage 3 criteria according to Brunnstorm Staging Participant conscious, oriented, on Glasgow coma scale above 12 Able to give written/verbal(recorded video-graphically) consent.

Exclusion criteria

Exclusion criteria: Stroke involving Basal Ganglia and Rigidity. Contractures after fibrosed muscles Pregnant and Lactating women Patients suffering from unstable Neurological condition Progressive stroke Participants requiring oxygen support Uncontrolled hypertension and/ or uncontrolled diabetes mellitus Known cases of malignancy, parkinsonism, Alzheimer disease, cases with pre-stroke spasticity conditions

Design outcomes

Primary

Measure	Time frame
To assess the change in muscle tone with the modified Ashworth Scale (MAS)Timepoint: (at baseline and at each follow up) Follow-up- weekly for first month and then fortnightly for 2nd to 6th month.	—

Secondary

Measure	Time frame
To assess the changes in pain at rest and pain evoked by passive joint movement by 11 point box test.Timepoint: (at baseline and during follow up weekly for first month and then fortnightly for 2nd to 6th month.;To assess the changes in the functional disability by The Barthel Index Score.Timepoint: at baseline and during follow up weekly for first month and then fortnightly for 2nd to 6th month;To assess the change in Quality of Life using Health Questionnaire-EuroQoL EQ-5D-5LTimepoint: at baseline,3 and 6 month	—

Measure

Time frame

To assess the changes in pain at rest and pain evoked by passive joint movement by 11 point box test.Timepoint: (at baseline and during follow up weekly for first month and then fortnightly for 2nd to 6th month.;To assess the changes in the functional disability by The Barthel Index Score.Timepoint: at baseline and during follow up weekly for first month and then fortnightly for 2nd to 6th month;To assess the change in Quality of Life using Health Questionnaire-EuroQoL EQ-5D-5LTimepoint: at baseline,3 and 6 month

—

Countries

India

Contacts

Public ContactDr Divya Taneja

Central Council for Research in Homoeopathy

renumittal8@gmail.com9717511115

Outcome results

None listed

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