To study the effect of ayurvedic formulation in Bed wetting.

A Single arm clinical Study to evaluate the efficacy of ayurvedic formulation in the management of shayyamutrata(Enuresis) - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/066572

Enrollment

Registered

2024-04-30

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Health Condition 1: N00-N99- Diseases of the genitourinary system Health Condition 2: F980- Enuresis not due to a substance orknown physiological condition Health Condition 3: F980- Enuresis not due to a substance orknown physiological condition

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: History of bed-wetting atleast twice in a week or more.

Exclusion criteria

Exclusion criteria: Patients with any known case of -CNS disorders, Epilepsy, 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
To decrease the frequency of bed wetting.Timepoint: 30 days study with follow up on 15th and 30th day (0,15,30 days)	—

Secondary

Measure	Time frame
To study the adverse effect of Ayurvedic Formulation ,if anyTimepoint: 30 days study with follow up on 15th and 30th day (0,15,30 days)	—

Countries

India

Contacts

Public ContactDr Mayuri Nemade

Dr. D.Y.Patil College of Ayurved and Research Centre

sbhagwat777@gmail.com7588562700

Outcome results