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Effect Of Nagaradi Granules In Balatisara (Diarrhea in children)

Clinical Evaluation Of Nagaradi Granules In Balatisara - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055275
Enrollment
50
Registered
2023-07-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Sponsors

Rishikul Campus
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Mild to moderate case of balatisara

Exclusion criteria

Exclusion criteria: Children below age of 5 years and above 16 years.

Design outcomes

Primary

MeasureTime frame
Relief in subjective parameters like - Muhur muhur pravriti (Frequency of stool), udarshoola (abdominal pain) and atidrava mala pravriti (consistency) Timepoint: The assesment will be done in the time period of 7 days on daily basis with the administration of drug and after 7 days without medication.

Secondary

MeasureTime frame
Relief in objective parameters like- Consistency & foul smellTimepoint: The assessment will be done in the time period of 07 days.

Countries

India

Contacts

Public ContactDr Keerti Verma

Rishikul Campus, Haridwar

keerti.vrm@gmail.com9997777833

Outcome results

None listed

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