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Effect of Vidangadi Syrup in Children with Intestinal Worm Infestation: A Randomized Controlled Study

Randomized Controlled Trial to Evaluate the Efficacy of Vidangadi Syrup in Pureeshaja krimi in Children - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112165
Enrollment
40
Registered
2026-06-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: B838- Other specified helminthiases

Interventions

None listed

Sponsors

Ankita Boniyal department of kaumarbhritya Uttarakhand Ayurved University Gurukul Campus Haridwar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients between the age group of 3-12 years irrespective of gender . 2.Primarily the patients will be selected on the basis of the presence of classical symptomatology of Pureesaja Krimi. Guda kandu (anal itching), shoola (abdominal pain), agnimandya (loss of appetite/weak digestion), panduta (pallor, anemia), karshya (weakness, reduced strength), (emaciation, weight loss), Pureeshbhed (loose stool) 3.Children with positive stool report for intestinal helminthes infestation. 4.Written informed consent from parents/guardians.

Exclusion criteria

Exclusion criteria: 1.Children with major congenital disorders and chronic debilitating diseases. 2.Patients with negative stool report of ova and cyst. 3.Children with severe anemia (Hb smaller than 7 g/dl). 4.Children with serious/systemic parasitic diseases such as hydatid cyst, neurocysticercosis, loffler s syndrome.

Design outcomes

Primary

MeasureTime frame
Parasitological cure rate of Pureeshaja Krimi infection assessed by stool examination (absence of ova/cysts) along with improvement in clinical symptoms after completion of treatmentTimepoint: The Assessment of patient will be done at 1st day, 7th day and 14th day.

Secondary

MeasureTime frame
Reduction in Guda Kandu (anal itching) Improvement in Agnimandya (loss of appetite) Reduction in Udarshoola (abdominal pain) Improvement in Pureeshbhed Improvement in Balakshaya and Karshya Improvement in PandutaTimepoint: 7th day, 14th day, and follow-up on 21st day.

Countries

India

Contacts

Public ContactDr Gp Garg

Institute

deepbhu10@gmail.com9013945535

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026