Radiological Study of PENG Block Depth (Tomo-PENG)

December 18, 2020 updated by: Centre Hospitalier Universitaire de Besancon

Observational Tomodensitometric Study of the Anatomical Landmarks Depth Required to Perform Femoral Nerve Block or PENG Block. The Tomo-PENG Study.

This study evaluates the depth of anatomical landmarks required in regional anaesthesia to perform either Femoral Nerve Block or PENG Block.

Measures will be performed on abdominal and pelvic computed tomography as part of daily routine patient care.

Study Overview

Detailed Description

PENG Block is a new approach in regional anesthesia for hip surgery. The anatomical landmarks used to perform PENG Block are deeper than those for Femoral Nerve Block. Nevertheless, depth required for PENG Block is not yet evaluated since it may vary between patients.

Daily routine abdominal and pelvic computed tomography allow such anatomical description.

Study Type

Observational

Enrollment (Actual)

101

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Besançon, France, 25000
        • Centre Hospitalier Universitaire

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients who had a CT scan in a single institution

Description

Inclusion Criteria:

  • All adult patients who have had a CT scan including visualization of the pelvis and who have expressed no opposition

Exclusion Criteria:

  • pregnancy
  • Subject presenting a pathology likely to modify the anatomical landmarks studied: ie pelvic fracture, psoas haematoma, previous pelvic surgery or hip prosthesis or femoral bypass

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
PENG Block depth
Time Frame: 1 hour after radiological examination
Measure of puncture depth required to achieve a PENG Block on CT Scann images
1 hour after radiological examination

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Femoral Nerve Block depth
Time Frame: 1 hour after radiological examination
Measure of puncture depth required to achieve a Femoral Nerve Block on CT Scann images
1 hour after radiological examination
puncture angle needed
Time Frame: 1 hour after radiological examination
Measure of puncture angle that would be required to achieve a PENG Block depth on CT Scann images
1 hour after radiological examination
needle length needed
Time Frame: 1 hour after radiological examination
Measure of needle length that would be required to achieve a PENG Block depth on CT Scann images
1 hour after radiological examination

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 8, 2020

Primary Completion (ACTUAL)

July 10, 2020

Study Completion (ACTUAL)

July 10, 2020

Study Registration Dates

First Submitted

March 31, 2020

First Submitted That Met QC Criteria

April 3, 2020

First Posted (ACTUAL)

April 7, 2020

Study Record Updates

Last Update Posted (ACTUAL)

December 21, 2020

Last Update Submitted That Met QC Criteria

December 18, 2020

Last Verified

December 1, 2020

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2020-495

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

In accordance with future institutional decisions

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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