To study to test the effectiveness of shayyamutrantak syrup in treating bedwetting(Nocturnal Enuresis) in childrens

A SINGLE ARM CLINICAL STUDY TO EVALUATE THE EFFICACY OF AYURVEDIC FORMULATION (SHAYYAMUTRANTAK SYRUP) IN THE MANAGEMENT OF SHAYYAMUTRATA WITH REFRENCE TO ENURESIS - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/04/108243

Enrollment

Registered

2026-04-13

Start date

Unknown

Completion date

Unknown

Last updated

2026-04-27

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 5 to 12years of either sex will be selected History of bedwetting at least twice in a week The patient whose parents are ready for his or her childs participation in clinical trial by giving informed written consent

Exclusion criteria

Exclusion criteria: Patients with any known case of CNS disorders Cerebral palsy Autism Epilepsy ADHD Spina Bifida Developmental delay Muscular dystrophy Hydrocephalous 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 formulations (SHAYYAMUTRANTAK SYRUP) in childrensTimepoint: 15 days study with the follow up on 7th and 15th day (0,07,15)	—

Secondary

Measure	Time frame
To study the adverse effect of Ayurveda Formulation(SHAYYAMUTRANTAK SYRUP)Timepoint: 15 days study with follow up on (0,7,15 days)	—

Countries

India

Contacts

Public ContactDr Jyotsna Ahir

LRP Ayurvedic Medical Colllege Hospital PG Institute and Research centre Urun Ishwarpur

drjyotsnaahir@gmail.com7276538181

Outcome results