To Study the Add on effect of Ayurvedic treatment and Conventional standard medical care in post stroke cases.

Efficacy of add on effect of Holistic Ayurvedic treatment and Conventional Standard medical care in post stroke cases: An Exploratory, Non-randomized Comparative controlled trial

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/06/054241

Enrollment

Registered

2023-06-21

Start date

Unknown

Completion date

Unknown

Last updated

2023-07-25

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

Conditions

Health Condition 1: I633- Cerebral infarction due to thrombosis of cerebral arteries Health Condition 2: I678- Other specified cerebrovascular diseases

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Post stroke management cases immediately after discharge (7-30 days) 2.NIHSS score from 5-14. 3.Age 21-70 yr. 4.Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study. 5. 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.Participation in any clinical trial in the last 3 months which if the investigator seems prudent to be considered an exclusion criterion. 2.Patients with unstable vitals or uncontrolled HTN & DM 3.Patients with other malignant conditions of brain 4.Any evidence of infectious conditions 5.Unwilling or unable to comply with the criteria in the Lifestyle Requirements section of this protocol. 6.Other acute or chronic medical or psychiatric condition including recent (within the past year) or active suicidal ideation or behavior or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study. 7.NIHSS 14 8.Hemorrhagic stroke

Design outcomes

Primary

Measure	Time frame
1.Improvement in the signs and symptoms of stroke. â?¢Symptoms of stroke 1.Paralysis/Weakness of upper limb 2.Paralysis/Weakness of lower limb 3.Difficulty for locomotion 4.Rigidity 5.Flaccidity 6.Spasm 7.Numbness 8.Head ache 9.Difficulty in speech 10.Pain in either half of the body 11.Incontinence / retention of urine 12.Incontinence/retention of Motion 13.Facial Palsy Timepoint: at presentation (Day 0), Day 15, Day 30, Day 60 & Day 90	—

Measure

Time frame

1.Improvement in the signs and symptoms of stroke. â?¢Symptoms of stroke 1.Paralysis/Weakness of upper limb 2.Paralysis/Weakness of lower limb 3.Difficulty for locomotion 4.Rigidity 5.Flaccidity 6.Spasm 7.Numbness 8.Head ache 9.Difficulty in speech 10.Pain in either half of the body 11.Incontinence / retention of urine 12.Incontinence/retention of Motion 13.Facial Palsy Timepoint: at presentation (Day 0), Day 15, Day 30, Day 60 & Day 90

—

Secondary

Measure	Time frame
1. Changes in QoL, SF-36 2. CBC, ESR, LFT, RFT, Vit-D, Vit-B12, Lipid profile, RBS, TFT(If done). 3. To evaluate the changes in Hamilton Anxiety Rating Scale (HAM-A) Timepoint: at presentation & Day 90	—

Countries

India

Contacts

Public ContactDr Alisha

All india Institute Of Ayurveda

jonahdr@gmail.com9448262298

Outcome results