NCT01080599

Brief 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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2009

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2009

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2010

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2010

Completed
29 days until next milestone

First Submitted

Initial submission to the registry

March 2, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 4, 2010

Completed
Last Updated

March 4, 2010

Status Verified

March 1, 2010

Enrollment Period

7 months

First QC Date

March 2, 2010

Last Update Submit

March 3, 2010

Conditions

Keywords

obturator nerve block in TURB

Outcome Measures

Primary Outcomes (1)

  • Assessment of obturator sign during using nerve stimulator and operation

Study Arms (2)

conventional pubic approach

EXPERIMENTAL
Procedure: obturator nerve block

inguinal approach

EXPERIMENTAL
Procedure: obturator nerve block

Interventions

conventional pubic approachinguinal approach

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 2, 2010

First Posted

March 4, 2010

Study Start

June 1, 2009

Primary Completion

January 1, 2010

Study Completion

February 1, 2010

Last Updated

March 4, 2010

Record last verified: 2010-03