A Study To Evaluate The Effect of tablet formed by the Samangadi kwath contents dravya In Diarrhoea In Pre-Shool Children

A Single Arm Open Labelled Clinical Trial To Evaluate The Efficacy Of Samangadi Kwath Ghan Vati In Baalatisara (Diarrhoea In Pre-School Children) - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084489

Enrollment

Registered

2025-04-09

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-28

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

Conditions

Health Condition 1: K928- Other specified diseases of the digestive system

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Children of age group of 3-6 years irrespective of caste, sex, religion. Patients lying under diagnostic criteria. Mild to moderate cases of diarrhoea. Patient suffering from mild level of dehydration. Parents of children are willing to participate in research trial.

Exclusion criteria

Exclusion criteria: Patients having age less than 3 years & above 6 year Patient suffering from moderate to severe dehydration Any serious life-threatening disease such as persistent vomiting severe dysentery and high grade fever Associated with severe systemic disease severe cases of diarrhoea

Design outcomes

Primary

Measure	Time frame
Reduction in the Number of Motions per Day: Assess the decrease in the frequency of bowel movements per day after administration of Samangadi Kwatha Ghan Vati over a specified period. It will be accessed on the basis of statistical analysis applied on Assessment parameters after completion of trial. It will be accessed on the basis of statistical analysis applied on subjective parameters after completion of trial.Timepoint: 14 days	—

Measure

Time frame

Reduction in the Number of Motions per Day: Assess the decrease in the frequency of bowel movements per day after administration of Samangadi Kwatha Ghan Vati over a specified period. It will be accessed on the basis of statistical analysis applied on Assessment parameters after completion of trial. It will be accessed on the basis of statistical analysis applied on subjective parameters after completion of trial.Timepoint: 14 days

—

Secondary

Measure	Time frame
1. Reduction in Abdominal Pain or Discomfort. 2. Improvement in Appetite and Digestion 3. Reduction in Associated Symptoms 4. General Well-being and Quality of LifeTimepoint: 14 days	—

Countries

India

Contacts

Public ContactAarti

Institute For Ayurveda Studies And Research, Kurukshetra

duggalaatul4@gmail.com8950683630

Outcome results