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A Single Arm Clinical Study on Amapachaka Effect of Takrasanskarita Rason in Individuals with Ama Lakshana using the Ama Assessment Score - nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/103890

Enrollment

Registered

2026-02-16

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: R688- Other general symptoms and signs

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Individual of both sexes between Age group 35-65 years 2 Individual with Ama Lakshana equal and more than 4 Lakshana measured by Ama Assessment score

Exclusion criteria

Exclusion criteria: 1 Individual having high grade fever more than 100 C 3 Individual having serious systemic disease 4 Individual with comorbidities bleeding disorders 5 Individual diagnosed with anorectal disease like hemorrhoid fissure fistula 6 Pregnant and lactating women 7 Individual having Infections

Design outcomes

Primary

Measure	Time frame
1.To Assess the changes in Aam Assessment score (WHO-Scoring of ayurveda symptoms) before and after consumption Takrasanskarit Rason Timepoint: 0 Week 1 Week 2 Week	—

Secondary

Measure	Time frame
1 To evaluate the effect on Agnibala of Takrasanskarit Rason as Dietary Modification. 2 To observe improvement in specific Ama Lakshana like strotorodh anilmudhata Timepoint: 0 Week 1 Week 2 Week	—

Countries

India

Contacts

Public ContactDr Priyanka Karbhari Bondare

Government Ayurved College and Hospital Nagpur

sumeetasjain@gmail.com9373111200

Outcome results