A clinical study comparing intracorpus spongiosum block and topical anesthesia for pain relief during surgery (internal urethrotomy) for urethral strictures
Not Applicable
- Conditions
- Health Condition 1: null- Urethral stricture disease
- Registration Number
- CTRI/2011/12/002287
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. Male patients 18 years or above.
2. Single passable anterior urethral stricture up to 2 cm of length.
Exclusion Criteria
?Multiple strictures.
?Stricture of fossa navicularis.
?Stricture length more then 2 cm.
?Known allergy to lignocaine.
?Associated urological co-morbidities like urethral or vesical calculus, benign prostatic hyperplasia, neurovesical dysfunction.
?Significant cardiovascular disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method