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NCT05163899 · ClinicalTrials.gov registry record · Phase 2

Investigation of Surgical Sectioning of the Filum Terminale in Treating Occult Tethered Cord Syndrome Patients

A Phase 2 study of Tethered Cord and Tethered Cord Syndrome, sponsored by Weill Medical College of Cornell University.

Recruiting
Registry status
Phase 2
Development phase
20
Enrollment target
1
Study location

NCT05163899 is a Phase 2 study of Tethered Cord and Tethered Cord Syndrome that is actively recruiting participants, run by Weill Medical College of Cornell University. The registered enrollment target is 20 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT05163899, a Phase 2 study of Tethered Cord and Tethered Cord Syndrome, is actively recruiting participants, sponsored by Weill Medical College of Cornell University.

RECRUITING
Registry status
Phase 2
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

The investigators hypothesize that surgical release of the filum terminale (strand of fibrous tissue at the end of the spinal cord) is a more efficacious treatment option for symptomatic relief than medical management in subjects with Occult Tethered Cord Syndrome (OTCS) and that the risks do not outweigh the benefit profile.

Interventions

  • PROCEDURE Release of filum terminale

Study Locations (1)

New York

  • Weill Cornell Medicine - New York

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2022-05-19
Est. Completion 2028-05
Phase Phase 2

What the Registry Record Tells You About NCT05163899

The ClinicalTrials.gov registry entry for NCT05163899 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Tethered Cord appearing as the primary indexed condition, and to 1 intervention - of which Release of filum terminale is the first listed.

NCT05163899 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT05163899 about?

NCT05163899 is a clinical study titled "Investigation of Surgical Sectioning of the Filum Terminale in Treating Occult Tethered Cord Syndrome Patients". The investigators hypothesize that surgical release of the filum terminale (strand of fibrous tissue at the end of the spinal cord) is a more efficacious treatment option for symptomatic relief than medical management in subjects with Occult Tethered Cord Syndrome (OTCS) and that the risks do not ou...

What is the current status of trial NCT05163899?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2022-05-19. Estimated completion is 2028-05.

What conditions does trial NCT05163899 study?

This clinical trial studies the following conditions: Tethered Cord, Tethered Cord Syndrome, Occult Spina Bifida, Spina Bifida Occulta.

What interventions are being tested in trial NCT05163899?

The interventions under investigation include: Release of filum terminale (PROCEDURE).

Who is sponsoring clinical trial NCT05163899?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05163899 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.