Comaparative clinical study of Patoladi Kwath and Kokilakshadi Kwath in Vatarakta (Gout)

Pharmaceutico-Analytical study of Kokilakshadi Kwath and Patoladi Kwath and Assessment of their comparative efficacy in Vatarakta(Gout)-A Randomised Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/075783

Enrollment

Registered

2024-10-24

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Health Condition 1: M249- Joint derangement, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients showing classical symptoms of Vatarakta – Sandhi Shoola, Sandhi Shotha, Sparsh Asahatvam, Raaga, Twak Vaivarnya , Vidaha , Stabdhata. 2.Male Patients having Uric acid greater than 7mg/dl & female patients havig Uric acid greater than 5.7 mg/dl

Exclusion criteria

Exclusion criteria: Patients having systemic disorders like cardiac diseases, Diabetes, SLE, RA, OA, TB, Psoriatic arthritis, & Renal disorders. Any other patients considered unfit for the trial.

Design outcomes

Primary

Measure	Time frame
1)Prepare Kokilakshadi Kwath and Patoladi Kwath. 2)Analyse Kokilakshadi Kwath and Katoladi Kwath w.s.r to Ayurvedic & Modern parameters. 3)Clinically assess the efficacy of Kokilakshadi Kwath & Patoladi Kwath in Vatarakta. Timepoint: Follow up will be taken on Day- 15,30 and 45	—

Secondary

Measure	Time frame
Not applicableTimepoint: Not applicable	—

Countries

India

Contacts

Public ContactDr Raman Belge

Shri Ayurved Mahavidyalaya Nagpur

ramanbelge@gmail.com9822879010

Outcome results