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Comparison of Obturator Nerve Block With Ultrasound Guidance and Anatomical Signs

M

Muğla Sıtkı Koçman University

Status

Unknown

Conditions

Bladder Tumor
Succesful Obturator Nerve Block
Bleeding

Treatments

Procedure: obturator nerve block

Study type

Interventional

Funder types

Other

Identifiers

NCT04638569
27/12/2019-19/VIII

Details and patient eligibility

About

Comparison of the obturator nerve block in patients undergoing transurethral resection due to bladder tumor, technically using ultrasound guided or blinded with anatomical signs.

Full description

The primary aim of this study is to compare the success rates of ONB techniques performed with ultrasound guided or blind technique. Its secondary purpose is to compare the effect of peroperative bleeding and control cystoscopy performed in the postoperative 3rd month on the presence of recurrent tumor.

Enrollment

116 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-II patients

Exclusion criteria

  • Tumors that disrupt the integrity of the bladder,
  • bladder floor tumors,
  • coagulation disorders,
  • motor in the lower limbs
  • with sensory disturbances,
  • uncooperative patients,
  • Known allergy to local anesthetics
  • patients with localized infection at the procedure site

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

116 participants in 2 patient groups

Ultrasound-guided obturator nerve block group
Active Comparator group
Description:
The ultrasound probe will be placed in the middle of the tuberculum pubis and femoral artery, 5-6 cm below the inguinal ligament, and 5 mL of 0.5% bupivacaine will be injected into the anterior and posterior branches of the ON with a needle.
Treatment:
Procedure: obturator nerve block
obtutaror nerve block with anatomical landmarks
Active Comparator group
Description:
In the second group, after the patient is placed in the lithotomy position, 1.5 cm lateral tuberculum pubis and 1.5 cm caudal will be marked and needle entry will be made and 0.5% bupivacaine will be injected with 10 mL.
Treatment:
Procedure: obturator nerve block

Trial contacts and locations

1

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Central trial contact

Eylem Yasar, MD; eylem yasar

Data sourced from clinicaltrials.gov

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