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Nerve Composition of Human Lumbar Dorsal Primary Rami and Its Medial Branch

Sponsor: University of Aberdeen

NCT ID: NCT05091112

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Spinal surgery (procedure), Histology (other)
How long the study runs
Study runs about 33 months (dates as stated)
About the drug or intervention
Spinal surgery — procedure: In participants who undergo elective lumbar spinal surgery and consented for research, the medial branch and dorsal rami will be harvested for histological analysis. · Histology — other: The harvested nerves will be fixed, cut into smaller sections.
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
20
Started
2022-03-08
Last checked
2024-12

Plain English Summary

What is this study?

  • • Testing a new treatment for lumbar facet arthrosis
  • • Clinical study - 20 participants
  • • The purpose of the study is to understand the composition of the nerves supplying the facet joints in low back

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with lumbar facet arthrosis

Where?

  • • Aberdeen - Woodend Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The purpose of the study is to understand the composition of the nerves supplying the facet joints in low back.

More detail

After written informed consent, the nerves supplying the facet joints - lumbar dorsal rami and its medial branches, will be harvested when they are exposed during spinal surgery. These nerves will be fixed, washed and further dissected to enable smaller sections. The cut section will be stained and subjected to analysis of overall cross-sectional area and presence of connective tissue sheaths under light microscope.

Lumbar Facet ArthrosisNerve Degeneration

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Be aged 18 or over
  • ✓be able to give agreement to take part
  • ✓scheduled to undergo lumbar spinal surgery

Who cannot take part

  • ✗Children under 18 years old
  • ✗Vulnerable adults
  • ✗Adults with incapacity
  • ✗Inability to provide agreement to take part
  • ✗History of previous spinal surgery
See the full criteria
Inclusion Criteria: * Be aged 18 or over * be able to give informed consent * scheduled to undergo lumbar spinal surgery Exclusion Criteria: * Children under 18 years old * Vulnerable adults * Adults with incapacity * Inability to provide informed consent * History of previous spinal surgery * history of previous RF ablation for low back pain * has COVID-19 or displaying symptoms of COVID-19

Where Is This Study? (1 UK site)

Woodend Hospital

Aberdeen AB15 6XS, United Kingdom

Recruiting
Site contact (verified)
Saravana Kanakarajan, MD FRCAPrincipal Investigator

How to Get in Touch

Saravanakumar Kanakarajan, MD FRCA

Sponsor contact

CONTACT

00 44 1224 553237 saravanakumark@abdn.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-12