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Evaluate the Efficacy of Utterbasti and Urethral Dilation in Urethral Stricture.

Phase 2
Conditions
Health Condition 1: N359- Urethral stricture, unspecified
Registration Number
CTRI/2022/10/046131
Lead Sponsor
DSSRAU Jodhpur Rajasthan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

(1). A substantial haemorrhage into the urinary tract.

(2). Pain and inflammation in the urethra.

(3). Patients who will give written consent.

(4). Patients with classical signs and symptoms of urethral stricture will be included in the trial.

Exclusion Criteria

(1). Urethral diverticulum.

(2). Periurethral abscess.

(3). Urethral fistula.

(4). Urinary tract infection

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1 Stricture will be removed and relief in painTimepoint: 8 weeks
Secondary Outcome Measures
NameTimeMethod
Relief from all the types of urethral stricture symptomsTimepoint: 8 weeks
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