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NCT07611058Completed

Inflammatory Response in Children Suffering From Tethered Cord

Study of Inflammatory Response in Children Suffering From Tethered Cord

Source: ClinicalTrials.gov · Last updated 28 May 2026

Brief summary (registry, in English)

Embryologic phenomenons that lead to dysraphisms are known, but pathophysiology remains questioned. It is supposed not to be a simple mechanistic dysfunction, and other biological phenomenons are implied in spinal cord damaging. Two main hypothesis are that manual deformation of the cells and mitochondrial membranes lead to energy deficiency and blood flow changes. On the other hand, considering traumatic spinal cord injuries (SCI), inflammation has been shown to have dramatic effects on spinal cord function and physiology. Indeed, all essays about SCI have demonstrated that the initial trauma leads to mechanical injury to cells, accompanied by damages of microvasculature, initiation of pro-apoptotic signaling and ischemia. Therefore, we could imagine that similar inflammatory processes can be implied in stretched spinal cord. In our review of literature, we found few papers highlighting the question of inflammation and CSF sampling.

Status (registry)
Completed
Study type
Interventional
Enrollment
32 (actual)
First submitted
13 Oct 2023
Start date
May 2024
Primary completion date
Jan 2026
Lead sponsor
University Hospital, Lille
NCT number
NCT07611058

What you commit to

  • Study type: Interventional
  • Participants enrolled: 32
  • From May 2024 to the primary completion date, Jan 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Chronic inflammatory disease,

Age

  • Patients over 18 years of age,

Other

  • Ongoing anti-inflammatory treatments,
  • No parental consent,

Who the study is looking for

  • Infants and children under 18 years of age
  • Carriers of an attached marrow: lipomatous fiilum, meningocele, myelomeningocele, myelolipoma,
  • Consent of the child's parents,
  • Socially insured patient,
  • Patient willing to comply with all study procedures and duration,

Age in the registry: - to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU de Lille
Coordinator of this site? Confirm its status
LilleFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.