Multimodal Imaging and Biospecimen Collection for Low Back Pain (LBPB)

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorPeking University Third Hospital

About this trial

This prospective cohort study investigates the neurobiological, genetic, and psychosocial mechanisms underlying acute and chronic low back pain (LBP). Core objectives include establishing a high-quality biobank to support future research in connectomics, genomics, and biomarker discovery, and identifying predictors of pain progression and treatment response.

The study will also assess the impact of comorbid conditions such as anxiety, depression, and sleep disturbances on pain perception and clinical outcomes. Longitudinal analyses will explore the dynamic interplay between emotion, cognition, sleep, and pain to inform precision, mechanism-based interventions.

Functional imaging will be used to examine brain responses to nociceptive modulation, aiming to identify neural circuits involved in pain chronification. By integrating multimodal data-including neuroimaging, neurophysiology, microbiota profiling, polysomnography, and molecular assays-the study will define LBP subtypes, with a particular focus on nociceptive, neuropathic, and nociplastic mechanisms. The ultimate goal is to establish prognostic biomarkers and advance personalized strategies for LBP prevention and treatment.

Eligibility criteria

Qualifiers

Adults aged 18 to 80 years.

Diagnosis of low back pain, defined as pain located between the lower costal margins and the gluteal folds, with or without leg pain.

Eligible for surgical or non-surgical treatments.

Willingness to undergo neuroimaging (fMRI), microbiota sampling, psychological assessments, and other related study procedures. Ability to provide written informed consent.

Disqualifiers

Severe neurological deficits requiring emergency surgery.

Antibiotic or probiotic use within the past 4 weeks. Suffering from digestive diseases such as irritable bowel syndrome, gastric ulcer, duodenal ulcer, etc.;

Diagnosed spinal infections, tumors, fractures, or inflammatory diseases (e.g., ankylosing spondylitis).

Known severe psychiatric disorders (e.g., schizophrenia, bipolar disorder) that would interfere with study participation.Head trauma; history of substance abuse.

Trial design

Treatments tested in this trial

  • Nerve Block
  • endoscopic spinal disecetomy
  • Medication
  • Psychotherapy

Treatment groups

360 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Peking University Third Hospital

Lead sponsor

National Natural Science Foundation of China

Collaborator