Effect of Parasurgical procedure of Preputial Dilatation in Phimosis

Assessment of Effect of Parasurgical procedure of Preputial Dilatation in Niruddha Prakash w.s.r.t. Phimosis : An Open Clinical Trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/08/093498

Enrollment

Registered

2025-08-22

Start date

Unknown

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

Health Condition 1: N471- Phimosis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: patient with congenital phimosis

Exclusion criteria

Exclusion criteria: pathological phimosis Congenital abnormality like hypospadiasis, Epispadiasis Patients with HIV, HbsAg, HCV positive Congenital kidney disorder, Juvenile diabetes. Patient suffering with severe systemic disease

Design outcomes

Primary

Measure	Time frame
To assess the effect of preputial dilatation in niruddha prakash w.s.r.t. phimosis Timepoint: 4 weeks	—

Secondary

Measure	Time frame
To assess the reliability of preputial dilatation in niruddha prakash w.s.r.t. phimosisTimepoint: DURATION OF STUDY: 30 days PREPUTIAL DILATATION ON: Day 0 CLINICAL ASSESSMENT DONE ON: 0,1st, 4th ,7 th & 30th day	—

Countries

India

Contacts

Public ContactDr Shilpak Sunil Sadgune

ymt ayurved and medical college and hospital

shilpak.sadgune999@gmail.com9503448573

Outcome results