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Nerve BlockNCT01080599

Comparison of the Success Rate of Two Approaches for Obturator Nerve Block in TURB (Conventional Pubic Approach [Labat Technique] and Inguinal Approach)

A study testing obturator nerve block in people with Nerve Block, run by Yonsei University.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to compare the success rate of two approaches for obturator nerve block in TURB (conventional pubic approach [Labat technique] and inguinal approach. Read more about this study

Who is it for?
Ages 20 years and older
Conditions the study is for
Nerve Block
What is being tested?
obturator nerve block
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
No sites listed yet
Study dates
Jun 2009to Feb 2010
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Scheduled to undergoing transurethral resection of bladder tumor during combined spinal anesthesia and obturator nerve block were included in the clinical study

Who cannot join

  • Patients with advanced cardiac and respiratory insufficiency
  • Allergy to local anesthetics
  • Preexisting neurologic deficits
  • Prior operation involving the hip and the inguinal region and bleeding tendency were excluded.

About this study

The purpose of this study is to compare the success rate of two approaches for obturator nerve block in TURB (conventional pubic approach [Labat technique] and inguinal approach.

Conditions
Nerve Block
Being tested
obturator nerve block
Keywords
obturator nerve block in TURB

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • obturator nerve blockProcedure or surgery

Study groups in NCT01080599
Study groupRoleWhat they receive
conventional pubic approachExperimentalNot described
Receives: Procedure: obturator nerve block
inguinal approachExperimentalNot described
Receives: Procedure: obturator nerve block

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Assessment of obturator sign during using nerve stimulator and operation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Mar 2010 (estimated)
  2. Study startJun 2009
  3. Primary completionJan 2010
  4. Study completionFeb 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Randomised
Intervention model
Parallel groups
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01080599
Sponsor's protocol ID
4-2009-0137
Status last verified
Mar 2010
First submitted
2 Mar 2010
Last updated
4 Mar 2010
Results posted
No

Questions about this trial

What is this clinical trial studying?

A study testing obturator nerve block in people with Nerve Block, run by Yonsei University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Mar 2010. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessment of obturator sign during using nerve stimulator and operation. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Mar 2010.

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