CClinicalTrials.gg
Status unknownNCT05579795Updated Nov 3, 2022

Surgical Management and Outcome of Tethered Cord Syndrome

An observational study in Tethered Cord Syndrome, sponsored by Assiut University. Status unknown. Open to participants aged 1 Year to 16 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-11-03.

Sponsored by Assiut University · Observational

The sponsor has not verified this record recently (last verified Nov 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
35
Ages
1 Year to 16 Years
Sex
All
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Study summary

The aim of this study is to assess surgical management and outcome of Tethered cord syndrome

Read the detailed description

Tethered cord syndrome (TCS) is a developmental abnormality of the neuroaxis which is usually diagnosed in childhood. The actual tethering has been attributed to a variety of pathologic entities, including a thickened tight filum terminale , intradural lipomas with or without a connecting extradural component, intradural fibrous adhesions, diastematomyelia, and adherence of the neural placode following previous closure of a myelomeningocele. However, sufficient differences in the mode of onset, clinical manifestations, and outcome exist between pediatric and adolescent patients with tethered cord to warrant a more detailed analysis of the adult syndrome. The most problematic technical consideration in surgery for the release of the tethered cord is how to preserve functioning neural elements and rebuild the dural sac to avoid CSF leak. The purpose of this study is to review causes of Tethered cord, clinical presentation, diagnostic tools, treatment options and outcome in school-aged children, adolescents, and young adults with Tethered cord.

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Conditions studied

  • Tethered Cord Syndrome
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In context

Neural Tube Defects

49 studies on the registry are indexed under Neural Tube Defects; 11 are open to participants now.

This study's planned enrollment of 35 is below the median of 123 across 22 observational studies indexed under Neural Tube Defects.

Browse Neural Tube Defects studies →

Lead sponsor

Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
1 Year to 16 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Males and Females below 16 years old with Tethered cord syndome

Inclusion criteria

  • Patients with Tethered cord syndrome presenting at our institute
  • Patients with spinal dysraphism
  • Lipomyelomeningocele with Tethered cord
  • patients presented with neurological deficit after lipomyelomeningocele repair due to Tethered cord
  • patients presented with neurological deficit after myelomeningocele repair due to Tethered cord
  • Diastematomyelia with Tethered cord - Tethered cord due to filum terminale.
  • Tethered cord due to fibrous adhesions

Exclusion criteria

Exclusion Criteria:

  • Asymptomatic Patients with Tethered cord discovered accidentally
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
35 participants (estimated)
Patient registry
No

Interventions

  • ProcedureDetethering of the spinal cord

    Release of the tethered spinal cord

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What researchers measure

Primary outcomes

  1. Motor power

    Outcome of Detethering of the Tethered spinal cord according to Motor power of the lower limbs 5 grades 0: No visible muscle contraction 1. Visible muscle contraction with no or trace movement 2. Limb movement, but not against gravity 3. Movement against gravity but not resistance 4. Movement against at least some resistance supplied by the examiner 5. Full strength

    Time frame: Two years

  2. Sensations

    Outcome of Detethering of the Tethered spinal cord according to the sensations of lower limbs , is there decreased sensations of lower limbs and if improved or not

    Time frame: Two years

  3. Sphincter's function

    Outcome of Detethering of the Tethered spinal cord according to is there urinary incontinence or stool incontinence and if improved or not

    Time frame: Two years

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Yes — The aim of this study is to assess surgical management and outcome of Tethered cord syndrome.

Supporting information: Csr

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05579795
Lead sponsor
Assiut University
Responsible party
Amr Gamal Hussein Mohamed (Principal Investigator, Assiut University) — Principal investigator
First posted
Oct 14, 2022
Start date
Nov 2, 2022 (estimated)
Primary completion
Nov 2, 2024 (estimated)
Completion
Dec 2, 2024 (estimated)
Last update
Nov 3, 2022

Study contacts

Amr Gamal Hussein, GP
Contact
amrgamalz@yahoo.com
01067651618 ext. +2

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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