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A randomized clinical trial comparing intracorpus spongiosum block versus intraurethral lignocaine in visual internal urethrotomy for short segment anterior urethral strictures

A Randomised clinical trial comparing intracorpus spongiosum block versus intraurethral lignocaine in visual internal urethrotomy for short segment anterior urethral strictures.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/11/010503
Enrollment
60
Registered
2017-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N35- Urethral stricture

Interventions

Intervention1: Intracorpus spongiosum block: 3 mL of 1% lidocaine will be slowly injected into the dorsal glans in at least 1 min with a 26 Gauge hypodermic needle. To avoid bleeding, the glans will b

Sponsors

Department of Urology Institute of PostGraduate Medical Education and Research and SSKM Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Male patients 18 years or above. -Single anterior urethral stricture up to 2 cm of length.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Pain perception with the help of Visual Analogue Scale.Timepoint: 1.Pain during the surgery (VIU) 2.One hour after the of surgery completed.

Secondary

MeasureTime frame
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. 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.

Countries

India

Contacts

Public ContactDr Deepak Kumar Biswal

Institute of Post-Graduate Medical Education and Research and S.S.K.M. Hospital

urologyipgmer@gmail.com03322041299

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026