Study of Shayyamutra (Enuresis) in children by using Aamravatadi granules

Evaluation of the Efficacy of Aamravatadi Granules in Shayyamutra (Enuresis) in children - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/085738

Enrollment

Registered

2025-04-28

Start date

Unknown

Completion date

Unknown

Last updated

2025-05-26

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

Conditions

Health Condition 1: N394- Other specified urinary incontinence

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patient with age group of 05 to 12 years of either sex will be selected. History of bed-wetting at least twice in a week The patient whose parents are ready to participate in clinical trial by giving informed written assent.

Exclusion criteria

Exclusion criteria: Patients other than 05 to 12 year age group. Patients with any known case of - CNS disordersEpilepsy Spina Bifida Diabetes Mellitus Diabetes Insipidus Urinary Tract Infections Any Obstruction in Lower Urinary Tract Like Posterior urethral valve stenosis, distal urethral stenosis.

Design outcomes

Primary

Measure	Time frame
The symptoms of Shayyamutra are expected to be reduced after the use of Ayurvedic formulation in children.Timepoint: 15 days study with follow up on 7th and 15th day (0,07,15)	—

Secondary

Measure	Time frame
To study the adverse effect of Aamravatadi Granules in Shayyamutra if anyTimepoint: 15 day study with follow up on 7th day and 15th day (0,07,15)	—

Countries

India

Contacts

Public ContactDr.Snehal Suresh Nigade

drdeepak77@rediffmail.com9923220055

Outcome results