A comparative study to evaluate the efficacy of Dashamoola shruta ksheera kashaya parisheka(pouring of medicated milk) as an add on therapy in acute pain relief along with kokilaksha kashaya in comparison to kokilaksha kashaya alone and the Prakriti based pain response in Vatarakta

An exploratory Randomised controlled trial to evaluate the efficacy of Dashamoolasruta ksheera kashaya parisheka as an add on therapy in acute pain relief along with kokilaksha kashaya in comparison to kokilaksha kashaya alone and the Prakriti based pain response in Vatarakta with special reference to gouty arthritis - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/01/100009

Enrollment

Registered

2026-01-01

Start date

Unknown

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

Health Condition 1: M255- Pain in joint

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Diagnosed cases of Vatarakta having the ACR- EULAR GOUT CLASSIFICATION CRITERIA score greater than or equal to 8 2.Presence of acute pain in affected joints(self reported pain score greater than or equal to 5 on the VAS scale 3.Age between 30 to 60 years. 4. Irrespective of gender 5. Willingness to participate and comply with trial procedures. 6. Able to give informed written consent.

Exclusion criteria

Exclusion criteria: 1.Chronic or uncontrolled systemic illnesses: Uncontrolled Diabetes Mellitus Known cases of Renal, cardiac, or hepatic failure 2.Known cases of osteoarthritis, Rheumatoid arthritis 3. Active skin infections, ulcers, or wounds at the site of Parisheka application. 4. Pregnancy or lactation. 5. Known hypersensitivity to milk application 6. Use of analgesics or anti-inflammatory drugs (NSAIDs, steroids) within the past 1 week. 7. Psychiatric illness interfering with consent or pain reporting.

Design outcomes

Primary

Measure	Time frame
1) Pain Improvement in VAS score 2) Tenderness Improvement in tenderness grading 4) Blood parameters Improvement in blood parameters 5) Improvement in Ayurvedic subjective parameters Timepoint: Intervention period: 7 Days Follow-up Schedule: Assessment of Subjective and objective parameter on Day 0 and on Day 8 post-intervention Follow up on Day 14	—

Secondary

Measure	Time frame
1)Prakruti based pain response to Dashamoolasruta ksheera kashaya parisheka as an add on therapy in acute pain relief along with kokilaksha kashaya in comparison to kokilaksha kashaya aloneTimepoint: Intervention period 7 Days Follow-up Schedule Assessment of Subjective & objective parameter on Day 0 & on Day 8 post-intervention Follow up on Day 14	—

Countries

India

Contacts

Public ContactDr Resmi BG

All India Institute of Ayurveda

resmibg.aiia@gmail.com9895361423

Outcome results