A randomized clinical trial comparing intracorpus spongiosumblock versus intraurethral lignocaine in visual internalurethrotomy for short segment anterior urethral strictures
Not Applicable
Completed
- Conditions
- Health Condition 1: N35- Urethral stricture
- Registration Number
- CTRI/2017/11/010503
- Lead Sponsor
- Department of Urology Institute of PostGraduate Medical Education and Research and SSKM Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Male patients 18 years or above.
-Single 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 Pain perception with the help of Visual Analogue Scale.Timepoint: 1.Pain during the surgery (VIU) <br/ ><br>2.One hour after the of surgery completed.
- Secondary Outcome Measures
Name Time Method Change of Systolic BP & Pulse rate during the surgery and 1 hour after surgery from baseline (pre-operative) value.Timepoint: 1.Maximum value during intraoperative period. <br/ ><br>2.At 1 hour post operative period.;Success of VIU will be measured at 6 months after the surgery (The procedure will be considered successful if the patient do not report any voiding difficulty and urethral calibration is easy with an 18F Foley catheter).Timepoint: 6 months post surgery.