Clinical trial to evaluate the efficacy of Shiroabhyanga with Ksheerabala taila in the management of Nidranash

Randomized Clinical trial to evaluate the efficacy of Shiroabhyanga with Ksheerabala taila in the management of Nidranash w.s.r to Insomnia - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084450

Enrollment

Registered

2025-04-09

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: F489- Nonpsychotic mental disorder, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient above 20 and below 60 years of age group 2.Patient of both the genders are included 3.Sleep disturbance occurs at least 3 times per week and has been problem for at least 1 month 4. Patient ready to give written informed consent

Exclusion criteria

Exclusion criteria: 1.Patients who are unfit for Abhyanga according to ayurvedic classics 2.Any patients suffering from known systemic illness or any chronic health disorder 3.Patients with Psychiatric diagnosis are excluded from this study were receiving any medication and drug that could cause sedation 4. Pregnant ladies and lactating mothers

Design outcomes

Primary

Measure	Time frame
To evaluate the efficacy of Ksheerabala Taila Shiroabhyanga in the management of Nidranash w.s.r to insomniaTimepoint: On 0th,7th,14th,21st day of trial.	—

Secondary

Measure	Time frame
1.To study the Nidranash and insomnia according to Ayurveda and modern science respectively in detail, along with mode of action of Shiroabhyanga. 2.To study Ksheerabala Taila in detail.Timepoint: On 0th 7th 14th 21st day of trial.	—

Countries

India

Contacts

Public ContactDr Tanuja Gaikwad

Late Kedari Redekar Ayurvedic Mahavidyalaya,Gadhinglaj

gaikwadtanuja14@gmail.com7588335343

Outcome results