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Assessment of Different Clinical Techniques to Treat Patients With Chronic Low Back Pain

Unknown statusNot applicableNCT06453291
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This clinical trial aims to assess the effectiveness of different clinical techniques in treating patients with chronic low back pain (CLBP). Two test groups will be included: one receiving conventional therapy (NSAIDs and other physical therapy techniques) and the other receiving a combination of neuromodulation and platelet-rich plasma (PRP) therapy. Chronic pain, persisting for more than three months, inhibits natural pathways like GABA and promotes excitatory pathways, leading to increased inflammation. The study hypothesizes that neuromodulation via the dorsal root ganglion (DRG) and PRP therapy will provide superior pain relief and functional improvement compared to conventional therapy.

Study details

Official title
Innovative Approaches in Managing Chronic Low Back Pain: A Comparative Assessment of Clinical Techniques
Interventions
  • Drug: NSAIDs (Nonsteroidal Anti-Inflammatory Drugs):
  • Procedure: Standard Physical Therapy
  • Procedure: Neuromodulation via Dorsal Root Ganglion (DRG):
  • Procedure: Platelet-Rich-Plasma Therapy
Sponsor
Iffat Anwar Medical Complex
Start date
2024-07-10
Primary completion
2025-04
Sex
All
Age range
from 40 Years to 60 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
Pakistan
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Adults aged 40-60 years. * Diagnosed with chronic low back pain persisting for more than three months. * Willingness to participate and comply with study procedures. * Ability to provide informed consent. Exclusion Criteria: * Comorbidities. * Contagious and Non-Contagious Infections * Known hypersensitivity to study interventions. * Presence of severe psychiatric disorders. * Pregnancy or breastfeeding. * Participation in another clinical trial within the last 30 days.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06453291