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Clinical study to compare effectiveness of ayurvedic medicine with ayurvedic procedure in primary insomnia.

A Clinical Study to Compare the effectiveness of Shiroabhayanga and Shirodhara with an Indigenous Herbal oil and Mamsyadi Kwath (Orally) in cases of Anidra w.s.r Primary Insomnia.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044736
Enrollment
50
Registered
2022-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: F510- Insomnia not due to a substance orknown physiological condition

Interventions

None listed

Sponsors

State Ayurvedic College and Hospital Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Individuals between the age group of 21 to 60 years of both sexes having insomnia of minimum one month duration will be selected randomly for the study. 2)Patients complaining of disturbed sleep with Athens insomnia scale (AIS) score >= 6

Exclusion criteria

Exclusion criteria: ï?¶ Patients below 21 years and above 60 years of age. ï?¶ Pregnant lady and lactating mother. ï?¶ Patients with major psychiatric illness like schizophrenia, depressive psychosis, epilepsy etc will not registered. ï?¶ Patients with alcohol dependency or drug dependency will excluded from the study. ï?¶ Patients having chronic illness like asthma, malignancies, liver cirrhosis, chronic renal failure, uncontrolled diabetes and Hypertension etc. will be excluded. ï?¶ Patients with acute illness like Congestive Cardiac Failure, Myocardial Infarction, Chronic Obstructive Pulmonary Disorders, meningitis, acute pain conditions and similar other disorders will be excluded.

Design outcomes

Primary

MeasureTime frame
Clinical outcome assessment among the people registered under the study will be done through 1.Athens Insomnia Scale (AIS) Score â?¥ 6 Nidranasha Angmarda,Shirogaurav,Jrimbha,Tandra,Bhrama,Apaki All the signs and symptoms are graded 0,1,2,3 on basis of intensity confirmed by clinical examination before trial.The clinical improvement during and after trial will also be correlated and assess with previous grading.Timepoint: 8 weeks.

Secondary

MeasureTime frame
Quality of life improvement.Timepoint: 8 weeks.

Countries

India

Contacts

Public ContactDr Rekha Bajpai

State Ayurvedic College and Hospital, Lucknow

dr.rekha2101@gmail.com9919339155

Outcome results

None listed

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