ClinicalTrials.Veeva

Menu

Explorative Proteomics in Pediatric Neuroborreliosis

Rigshospitalet logo

Rigshospitalet

Status

Active, not recruiting

Conditions

Pediatric Infectious Disease
Neuroborreliosis
Facial Palsy

Treatments

Diagnostic Test: Proteomics

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to use proteomic analysis to diagnose Lyme Neuroborreliosis (LNB) in children. Pediatric patients with suspected LNB will be enrolled, and their blood samples will be collected for proteomic analyses. Mass spectrometry will be used to compare protein profiles of LNB-positive and LNB-negative patients. The data will be analyzed by bioinformaticians. The expected impact is to establish a non-invasive, reliable method for early LNB diagnosis to improve patient outcomes.

Full description

Objective:

The primary objective of this study is to investigate the utility of proteomic analysis in diagnosing lyme neuroborreliosis (LNB) in children. By identifying specific protein markers associated with LNB (proteomics), the investigators aim to enhance early detection and improve patient outcomes.

Methods:

Participant Recruitment:

The investigators will enroll pediatric patients (aged 1 month to 17 years) presenting with suspected LNB.

Informed consent will be obtained from parents or legal guardians.

Sample Collection:

Peripheral blood samples will be collected from each participant in EDTA tubes. Samples will be processed to carry out proteomic analyses.

Proteomic Analysis:

Mass spectrometry will be employed to compare protein profiles between LNB-positive and LNB-negative patients.

Data Analysis and Presentations:

Protein profiles will be analysed by trained bioinformaticians and mainly presented in volcano plots and heat maps.

Outcome Measures:

Unique proteomic profiles of children with LNB.

Expected Impact:

This study aims to establish a non-invasive and reliable method for diagnosing LNB in children. Early identification will facilitate timely treatment and prevent complications associated with LNB.

Enrollment

106 patients

Sex

All

Ages

1 month to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Presenting at a pediatric ward with facial nerve palsy and/or suspicion of lyme neuroborreliosis
  • Parental informed consent

Exclusion criteria

  • Parents or legal guardians unable to understand given information or comply with study criteria
  • Patient unable to cooperate to study procedures (blood sample)
  • Unclear etiology after lumbar puncture

Trial design

106 participants in 2 patient groups

Children with neuroborreliosis
Treatment:
Diagnostic Test: Proteomics
Children without neuroborreliosis
Treatment:
Diagnostic Test: Proteomics

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems