To study the effect of haritaki taila nasya in Akala palitya that is premature greying of hair.

Randomised Open Controlled Clinical Study To Evaluate The Efficacy Of Haritaki Taila Nasya In The Management Of Akala Palitya. - Nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/11/097948

Enrollment

100

Registered

2025-11-24

Start date

Unknown

Completion date

Unknown

Last updated

2025-12-08

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Subjects who are willing to participate in the study Subjects indicated for nasya karma. Irrespective of gender and religion.

Exclusion criteria

Exclusion criteria: Subjects suffering from skin diseases or any of the systemic diseases Subjects with K/H/O anaemia or any other autoimmune diseases. Subjects with K/H/O hormonal diseases or any hereditary disorder. Subjects with age above 34 years. Lactating mothers, female planning to conceive. Subjects contraindicated for Nasya Karma.

Design outcomes

Primary

Measure	Time frame
To study the efficacy of Haritaki Tail Nasya for 90days in Akala Palitya .Timepoint: 90 Days	—

Secondary

Measure	Time frame
To reduce the signs and symptoms of Akala Palitya. To assess the improvement by signs, symptoms & gradation of assessment criteria. To study etiopathology & clinical manifestation of Akala Pality. To improve quality of life and reduce discomfort of Patients. To achieve the outcome of study in 3 months.Timepoint: 90 Days	—

Countries

India

Contacts

Public ContactDr Gauri Ramakant Nake

Yashwant Ayurvedic College Post Graduate Training and Research Centre Kodoli

sukanyapatil250@gmail.com7406934574

Outcome results