PunctureCube: Comparison of a New Needle Navigation Device for CT-guided Interventions to the Conventional Free-hand Method

Sponsor
Luca Remonda (Other)
Overall Status
Recruiting
CT.gov ID
NCT04809298
Collaborator
(none)
120
1
2
43
2.8

Study Details

Study Description

Brief Summary

In a prospective, randomized, controlled, parallel group study the accuracy, intervention time and radiation dose of CT-guided punctures using the Puncture Cube® will be compared to the conventional free-hand method in patients requiring a percutaneous diagnostic or therapeutic CT-guided intervention for lumbar pain (facet joint-, nerve root-, epidural infiltrations at the lumbar/lumbosacral level).

Condition or Disease Intervention/Treatment Phase
  • Device: Free-hand therapeutic CT-guided punction for lumbar pain
  • Device: Puncture Cube
N/A

Detailed Description

Computed tomography (CT)-guided interventions for diagnostic and therapeutic purposes are standard approaches in clinical routine (e.g. in patients with low back pain). Numerous CT needle navigation systems have been developed with the aim to improve accuracy (and thus safety) of punctures while decreasing radiation exposure and procedure time. Their usability in clinical routine is limited either because of high sensitivity to interference, high expenses, bulkiness, or incompatibly with daily clinical practice and thus increasing procedure time and workflow complexity. The Puncture Cube® takes into account all these requirements. Furthermore, in an in vitro-phantom study (study submitted for publication), punctures with the Cube were found to be faster and more accurate compared to the free-hand conventional method.

In a prospective, randomized, controlled, parallel group study the accuracy, intervention time and radiation dose of CT-guided punctures using the Puncture Cube® will be compared to the conventional free-hand method in patients requiring a percutaneous diagnostic or therapeutic CT-guided intervention for lumbar pain (facet joint-, nerve root-, epidural infiltrations at the lumbar/lumbosacral level).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Prospective, randomized, controlled, parallel group studyProspective, randomized, controlled, parallel group study
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Prospective, Randomized, Controlled, Parallel Group Study to Compare a New Needle Navigation Device for CT-guided Interventions to the Conventional Free-hand Method
Actual Study Start Date :
Jun 1, 2019
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Free-hand lumbar punction

Diagnostic or therapeutic CT-guided intervention for lumbar pain management using the free-hand method.

Device: Free-hand therapeutic CT-guided punction for lumbar pain
Diagnostic or therapeutic CT-guided intervention for lumbar pain management using the Puncture Cube® as a needle navigation device.

Active Comparator: Puncture Cube

Diagnostic or therapeutic CT-guided intervention for lumbar pain management using the Puncture Cube® as a needle navigation device.

Device: Puncture Cube
Diagnostic or therapeutic CT-guided intervention for lumbar pain management using the Puncture Cube® as a needle navigation device.

Outcome Measures

Primary Outcome Measures

  1. Puncture accuracy [during procedure time approximately 30 min.]

    Assessment of puncture accuracy (distance and angle error between planned and achieved trajectory)

Secondary Outcome Measures

  1. Number of control acquisitions to achieve target [during procedure time approximately 30 min.]

    Number of control acquisitions to achieve target

  2. Assessment of radiation dose [during procedure time approximately 30 min.]

    Assessment of radiation dose

  3. Assessment of intervention time [during procedure time approximately 30 min.]

    Assessment of intervention time

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients requiring a percutaneous therapeutic CT-guided intervention for

  • lumbar pain (joint-, nerve root-, epidural infiltrations at the lumbar/lumbosacral level)

  • age ≥ 18 years

  • Signed informed consent prior to intervention

Exclusion Criteria:
  • Patients suffering from severe obesity (BMI > 30 kg/m2)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Neuroradiology, Kantonsspital Aarau Aarau Aargau Switzerland 5001

Sponsors and Collaborators

  • Luca Remonda

Investigators

  • Principal Investigator: Luca Remonda, Prof., Department of Neuroradiology, Kantonsspital Aarau

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Luca Remonda, Prof. Dr. med., Kantonsspital Aarau
ClinicalTrials.gov Identifier:
NCT04809298
Other Study ID Numbers:
  • Puncture Cube
First Posted:
Mar 22, 2021
Last Update Posted:
Apr 7, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 7, 2022