Comparative study of Rasnadi Tail drops nasya and Shadbindu Tail drops nasya in Headache.

Randomised comparative clinical trial to study the efficacy of Rasnadi Tail Nasya and Shadbindu Tail Nasya in Vataja Shirashoola

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/12/022564

Enrollment

Registered

2019-12-30

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: R51- Headache

Interventions

Intervention1: Rasnadi Taila Nasya: 2-2drops per day in each nostril for 7days Control Intervention1: Shadbindu Taila Nasya: 2-2 drops per day in each nostril for 7days

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient suffering from symptoms of Vataj Shiroshoola irrespective of time period 2) Patient between age group 20 to 60 years 3)Patient of either gender.

Exclusion criteria

Exclusion criteria: 1)Patients who have known cases of hypertension and dibetes. 2)Secondary headache caused by known cases of meningitis,tumor,encephalitis and refractive errors. 3) Known cases of pregnancy and lactation.

Design outcomes

Primary

Measure	Time frame
Subjective criteria (by using grades and analouges pain scale) Bhrama (giddiness) Shastra arni nibha (Throbbing pain) Objective criteria (gradation) 1) Severity of headache 2)frequency of headache 3)duration of headacheTimepoint: 21 days	—

Secondary

Measure	Time frame
Study the concept of vataj shiroshoola and headache in details Study the Nasya kriya kalpa and its uses,indications,contra indications and the complications.Timepoint: 21 days	—

Countries

India

Contacts

Public ContactDrVinayak Anaji Sirsat

MAMs Sumatibhai Shaha Ayurved College

drnspradhan@yahoo.com9423580963

Outcome results

None listed

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