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Comparison of Interfascial Injection Versus Subpectineal Injection on Ultrasound-guided Obturator Nerve Block

Not Applicable
Completed
Conditions
Bladder Neoplasm
Interventions
Procedure: Subpectineal Injection
Procedure: Interfascial Injection
Registration Number
NCT05540847
Lead Sponsor
Diskapi Teaching and Research Hospital
Brief Summary

This study aimed to assess the effectiveness of the ultrasound-guided interfascial injection approach with the subpectineal injection technique for obturator nerve block in bladder cancers undergoing transurethral resection of bladder tumor (TURBT) under spinal anesthesia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Lateral wall bladder tumour
  • ASA I-II patients
Exclusion Criteria
  • Contraindications for spinal anesthesia,
  • Tumors that disrupt the integrity of the bladder,
  • Coagulation disorders,
  • Uncooperative patients,
  • Allergy to local anesthetics.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Ultrasound guided subpectineal obturator nerve blockSubpectineal InjectionIn supine position, the ultrasound probe will be placed on in inguinal region, 1-2 cm below to the inguinal crease to identiy the subpectineal area. Patients in this group will receive subpectineal obturator nerve block under ultrasound guidance.
Ultrasound guided interfascial obturator nerve blockInterfascial InjectionIn supine position, ultrasound probe will be placed on inguinal region, 2-3 cm below to the inguinal crease. Patients in this group will receive interfascial obturator nerve block under ultrasound guidance.
Primary Outcome Measures
NameTimeMethod
Success rate of obturatr nerve blockPeroperative period

The success or fail of the obturator nerve block will be conformed using nerve stimulator. Detecting muscles twitch will br considered to be a fail.

Secondary Outcome Measures
NameTimeMethod
Procedure timeDuring the procedure

Block performance time will be recorded from the time the first ultrasound image is obtained until the procedure is completed

Sensory block30 minutes after the intervention

Sensory block area will be evaluated by a pin prick at in the dermatomal areas related obturator nerve and branches.

Patient satisfactionPeroperative period

Changes in overall satisfaction will be assessed using a 5 point Likert Scale ( 1-very dissatisfied, 2- dissatisfied, 3- neutral, 4-satisfied, 5 - very satisfied

Number of adductor muscle spazmsIntraoperative period

Number of adductor muscle spazms in each group will be noted during the intraoperative period.

Trial Locations

Locations (1)

Health Science University Diskapi Yildirim Beyazıt Training and Research Hospital

🇹🇷

Yenimahalle, Ankara, Turkey

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