The First Puncture Success Rate of a Novel Injeq IQ-Tip™ System in Pediatric Lumbar Punctures (IQ-LP-03)

The investigation aims to demonstrate the first puncture success rate, as proxy of clinical benefit and clinical performance, of bioimpedance spectroscopy based spinal needle guidance method among pediatric hemato-oncology patients requiring lumbar punctures.

Study Overview

• Status: Completed
• Conditions: Lumbar Puncture
• Intervention / Treatment: Device: IQ-Tip(tm) system

Detailed Description

The primary purpose of the investigation is to demonstrate the claimed clinical benefit and safety of Injeq IQ-Tip™ system.

IQ-Tip™ is similar to common spinal needles with a custom-made stylet that enables the real-time bioimpedance measurement at the tip of the needle. The needle is connected to the analyzer device, which provides real-time CSF detection during lumbar puncture from the very tip of the needle and by these means assists conducting the medical procedure.

The investigation aims to demonstrate the first puncture success rate, as proxy of clinical benefit and clinical performance, of bioimpedance spectroscopy based spinal needle guidance method among pediatric hemato-oncology patients requiring lumbar punctures.

The investigation is conducted in the pediatric hematology and oncology units of three Finnish university hospitals

• Study Type: Interventional
• Enrollment (Actual): 50
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Finland
  • Helsinki, Finland
    • Helsinki University Hospital, New Children's Hospital
  • Tampere, Finland
    • Tampere University Hospital
  • Turku, Finland
    • Turku University Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 1 year to 18 years (Child, Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Pediatric hemato-oncology patients whose diagnosis or treatment plan requires lumbar puncture to acquire a CSF sample or to inject drug or other substance
• Written and signed informed consent before the procedure from the parent and/or patient depending on the age of the patient

Exclusion Criteria:

• Parents and/or patient refusal to participate or parents and/or patient unable to give informed consent
• Any contraindications to a lumbar puncture. Contraindications include skin infection around the puncture area, unstable hemodynamics, bleeding tendency and increased intracranial pressure

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: IQ-Tip; At most four lumbar punctures with Injeq IQ-Tip(tm) system per participant	Device: IQ-Tip(tm) system; Physician performs therapeutic or diagnostic lumbar puncture using Injeq IQ-Tip(tm) system

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The First Puncture Success Rate	Each individual lumbar puncture procedure is assessed as either 'first puncture success' or '-failure'. Success rate = Successes / All procedures Definition of the first puncture success: Only one skin puncture with the needle is allowed;; Multiple stylet removals and reinsertions are allowed;; Multiple needle reorientations are allowed as long as needle tip remains inside the skin;; Physician must be able obtain a cerebrospinal fluid (CSF) sample that is sent to a laboratory analysis or to inject the intended medication to the patient's subarachnoid space; and; Physician conducting the puncture remains the same during the procedure	The assessment immediately following each lumbar puncture procedure
Rate of Serious Adverse Events	Total number of serious adverse events caused by the device. Serious adverse event in probable or causal relationship to the investigational device exposure	The assessment during four-week follow-up after each lumbar puncture procedure

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Percentage of Procedures With Post-dural Puncture Headache (PDPH)	PDPH defined as headache that: worsens in sitting or standing position; eases when lying down; occurs within 7 days after the lumbar puncture procedure Possible symptoms are recording using a diary filled by the patient or parents and verified by the study nurse.	The assessment during 7-day follow-up after each lumbar puncture procedure
Percentage of CSF Samples With Greater or Equal to 10 Erythrocytes / mm^3	Erythrocyte (red blood cell) count according to laboratory analysis in units of 10^6/liter or 1/mm3	The laboratory analysis within 3 hours of the lumbar puncture
Percentage of Procedures With Other Complications or Adverse Events	E.g. PDPH or backache Possible symptoms are recorded using a diary filled by the patient or parents and verified by the study nurse. Diary is an open questionaire that is intended for recording any possible complication. Possible complications are not considered as pre-determined outcome measures, with the exception of Outcome #3 (rate of PDPH) Four-week follow up conducted by the study nurse from the hospital registers	The assessment during 7-day and four-week follow ups
Aggregate Sensitivity of CSF Detection	The CSF detection performance of the investigational device is assessed by the physician. Each individual lumbar puncture procedure is classified as either 'True Positive CSF detection (TP)', 'False Negative CSF detection (FN)' or 'Procedure failed (Fail)' by the investigator. The aggregate sensitivity = Number of TPs / Total number of procedures	The assessment immediately following each lumbar puncture procedure
Aggregate False Detection Rate of CSF Detection	Each individual lumbar puncture procedure is classified as either 'One or more False Positive CSF detections (FP)' or 'No False Positive CSF detections (TN)'. The aggregate false detection rate = Number of FPs / Total number of procedures	The assessment immediately following each lumbar puncture procedure
Number of Required Attempts Per Successful Lumbar Puncture Procedure	In line with definition of 'the first puncture success rate', attempt is defined as: any new penetration of skin is considered a new attempt. Lumbar puncture is considered successful irrespective of the number of punctures if the CSF sample was eventually obtained and/or the injection of medicine could be performed	The assessment immediately following each lumbar puncture procedure
Number of Failed Lumbar Puncture Procedures	Procedure is considered failed if physicians, even after multiple attempts, conclude that the lumbar puncture cannot be completed with available personnel or equipment due to any reason	The assessment immediately following each lumbar puncture procedure

Collaborators and Investigators

• Sponsor: Injeq Ltd
• Investigators: Principal Investigator: Sauli Palmu, PhD MD, Tampere University Hospital

Study record dates

Study Major Dates

• Study Start (Actual): November 8, 2019
• Primary Completion (Actual): August 6, 2020
• Study Completion (Actual): October 2, 2020

Study Registration Dates

• First Submitted: August 23, 2019
• First Submitted That Met QC Criteria: August 26, 2019
• First Posted (Actual): August 28, 2019

Study Record Updates

• Last Update Posted (Actual): June 13, 2023
• Last Update Submitted That Met QC Criteria: June 12, 2023
• Last Verified: June 1, 2023

More Information

Terms related to this study

• Keywords: Lumbar puncture; Spinal puncture
• Additional Relevant MeSH Terms: Wounds and Injuries
• Other Study ID Numbers: IQ-LP-03

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No