A study to find the effectiveness of Sanjeevi Thailam (External-oil bath) and Plain Amukkara chooranam (Internal) with Sanjeevi Thailam(External-oil bath)in the management of Thookaminmai(Insomnia).

A Clinical Trial to evaluate the effectiveness of Sanjeevi Thailam (External-oil bath) and Plain Amukkara chooranam (Internal) with Sanjeevi Thailam(External-oil bath)in the management of Thookaminmai(Insomnia)among out-patients attending Ayothidoss Pandithar Hospital, National Institute of Siddha. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/068776

Enrollment

Registered

2024-06-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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

Intervention1: Sanjeevi Thailam and Sanjeevi Thailam with Plain Amukkara Chooranam: 70 ml of oil for external oil bath per week for 48 days and 70 ml of oil for external oil bath per week for 48 days

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age between 18 - 80 years. 2.Sex: Male, Female 3.Students, Faculties, Workers in National Institute of Siddha. 4.Attenders of participants visiting OPD. 5.Pittsburgh Sleep Quality Index 15(Global PSQI) from 5 to 21 will be included. assessment, pittsburgh psqi.doc 6.Participants who are willing to sign the written Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1.Shift Workers, Drivers, Drug users. 2.K/C/O Participants with uncontrolled Hypertension. 3.K/C/O Diabetes 4.K/C/O Sinusitis 5.K/C/O Chronic renal failure 6.K/C/O Coronary artery disease 7.K/C/O Depression 8.Pregnancy and lactation 9.Malignancy

Design outcomes

Primary

Measure	Time frame
To compare the reduction in the scores by 25-50% of Insomnia participants between groups A and B (before and after treatment) using the Pittsburgh Sleep Quality Index.Timepoint: Raw drug selection 15 days Medicine preparation 15 days Patient selection 1 month Treatment plan 45 days Data collection 1 month Data analysis 1 month	—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDR LAKSHMIKANTHAM T

National Institute of Siddha

drlakshmiramaswamy@gmail.com9025575185

Outcome results

None listed

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