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Effect Of Combined Therapy With Ekangavir Rasa-Vaitaran Basti-Shirobasti In Pakshavadh.

Randomized Comparative Study On Ekangavir Rasa-Vaitaran Basti-Shirobasti in Combination on Barthel Index And NIH Stroke Scale in Pakshavadh with Special reference to Cerebral Infarction.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/016872
Enrollment
60
Registered
2019-01-03
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: G819- Hemiplegia, unspecified Health Condition 2: G811- Spastic hemiplegia Health Condition 3: G811- Spastic hemiplegia

Interventions

Intervention1: Ekangavir Rasa 125 mg/ B.D. Shudha Gandhak,Parad Bhasma, Kataloha Bhasma,Vanga Bhasma,Naga Bhasma,Tamra Bhasma,Abhrak Basma ,Tikshnaloh Bhasma,Shunthi,Pimpali,Marich. 2)Vaitarana Basti

Sponsors

Govenment Ayurved College Nagpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having signs and symptoms of hemiplegia i.e. Pakshavadh mentioned in Ayurvedic texts. 2. Patient having muscle power grade less or equal to 3 3. Patients of hemiplegia i.e. Pakshavadh due to cerebral thrombosis. 4. Patients of hemiplegia i.e. Pakshavadh of duration not more than 5 years. 5. Patients of either sex aged between 21 years -70 year. 6. Patient willing and able to participate in the study. 7. Patients who have not participated in any research project in last 6 months. 8. Patients of hemiplegia i.e. Pakshavadh having controlled hypertension (systolic upto140 mm of Hg and diastolic up to 90 mm of Hg) and diabetes mellitus (BSL fasting up to 130 mg/dl and Post Prandial up to 180 mg/dl).

Exclusion criteria

Exclusion criteria: 1.Patients of cerebral infraction due to atrial fibrillation, embolic stroke, carotid occlusion, cerebellar stroke and haemorrhagic stroke will be excluded. 2.Patients having seizers, hydrocephalous, pulmonary embolism, dysphagia, M.I., cardiac arrhythmia and septicaemia will be excluded. 3.Patients who have lost bowel and bladder control. 4.Patients having acute progressive cerebral infarction 5.Comatose and unconscious patients. 6.Patients having age 70 years will be excluded. 7.Patients having intra cranial infection, encephalitis and meningitis etc. 8.Patient having trauma, cerebral tumour, cerebral abscess. 9.Patient with congenital heart diseases like POA, ASD, VSD and FOD. 10.Patients contraindicated for Abhyanga like skin diseases, infective disease will be excluded. 11.Patients not fit for Basti. 12.Pregnant and lactating mothers.

Design outcomes

Primary

MeasureTime frame
1.To evaluate the effect of Ekangavir Rasa, Vaitarana Basti and Shirobasti in combination on Barthel Index and NIH Stroke Scale of Pakshavadh with special reference to Cerebral Infarction. 2.To evaluate the effect of Ekangavir Rasa with Vaitarana Basti on Barthel Index and NIH Stroke score of Pakshavadh with special reference to Cerebral Infarction.Timepoint: 1) For trial Group Snehan Svedan with Til tail, Vaitarana Basti along with Shirobasti given for 16 days and Ekangavir Rasa 125 mg for 30 days 2) For Control Group Snehan Svedan with Til tail, Vaitarana Basti given for 16 days and Ekangavir Rasa 125 mg for 30 days 3) On day zero which will be termed as B.T. Value, second assessment will be done on 17th day and Final Assessment will be done on 31st day.

Secondary

MeasureTime frame
To review and study literature of Pakshvadh.Timepoint: one and half year.

Countries

India

Contacts

Public ContactAshish Thatere

Government Ayurved College Nagpur

ashish.thatere@gmail.com9423406821

Outcome results

None listed

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