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To study the effect of Shankhapushpi and Jatamansi siddha taila Shirodhara on Anidra

RANDOMIZED CONTROLLED TRIAL OF SHANKHAPUSHPI AND JATAMANSI SIDDHA TAILA SHIRODHARA IN ANIDRA - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084349
Enrollment
80
Registered
2025-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: G470- Insomnia

Interventions

None listed

Sponsors

PMTs Ayurveda College, Shevgaon
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with signs and symptoms of Anidra , As per DSM-5 Criteria for Insomnia Diagnosis and as per PSQI scale. Irrespective of their sex, race & religion and economic status barrier.

Exclusion criteria

Exclusion criteria: Participants suffering from any psychiatric disorder or any major medical illness requiring significant care. Pregnant women. Patient undergone Shirodhara procedure prior to screening. Any known allergy to the treatment components.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of Shankhapushpi and Jatamansi siddha taila Shirodhara in Anidra. Is there any reduction in symptoms or frequency of symptoms of ANIDRA (insomnia) that will be assessed after 14 days.Timepoint: 7 day treatment with 3 follow up 0, 7, and 14th day

Secondary

MeasureTime frame
To review Anidra (Insomnia) in detail from Ayurveda and modern perspective. To evaluate the effect of Tila taila Shiroabhyanga in Anidra (Insomnia). To compare the effect of Shirodhara with Shankhapushpi and Jatamansi siddha taila and Shirobhyanga with Tila taila in Anidra. To observe adverse effect of drugs during the procedure.Timepoint: 7 day treatment with 3 follow up 0, 7, and 14th day

Countries

India

Contacts

Public ContactDr Sachin Gandhi

PMTs Ayurveda College, Shevgaon

arihantsai977@gmail.com9423389866

Outcome results

None listed

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