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?Patient-Reported Outcomes and Prognostic Factors Following Tethered Cord Release in Tethered Cord Syndrome: A Prospective Cohort Study

Patient-Reported Outcomes and Prognostic Factors Following Tethered Cord Release in Tethered Cord Syndrome: A Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112482
Enrollment
Unknown
Registered
2025-11-14
Start date
2025-11-17
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tethered Cord Syndrome

Interventions

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 6 years 2. Meet the clinical-radiological diagnosis criteria of TCS. Have at least one of the following radiological evidence: low conus (usually 2 mm or fatty signal), traction caused by spinal cord lipoma/adhesions, adhesion signs resulting from previous surgery; and combine at least one clinical manifestation (such as lumbosacral/lower limb pain, lower limb sensory/motor disorder, gait abnormality, urinary and fecal function disorder, etc.). 3. Have not received spinal cord tethering surgery before. 4. Can independently complete or complete the subjective scale with the assistance of a guardian. 5. Sign a written informed consent, and the patient/ guardian agrees to the surgery and participates in the clinical study.

Exclusion criteria

Exclusion criteria: 1. Inability to complete the subjective assessment scales or adhere to the follow-up schedule as required by the study protocol. 2. Presence of concomitant neurological disorders capable of independently causing symptoms similar to TCS and which are uncontrolled during the study period (e.g., acute/active myelitis, progressive neurodegenerative diseases, acute brain or spinal cord injury, space-occupying lesions). 3. Contraindication to or inability to undergo general anesthesia with endotracheal intubation.

Design outcomes

Primary

MeasureTime frame
Klinge 15-item scale scores;PedsQL Spinal Cord Injury Module scores;

Secondary

MeasureTime frame
PHQ-9/GAD-7 scores;Physical examination scale scores;

Countries

China

Contacts

Public ContactZheng Wenjian

Shenzhen Second People's Hospital

fish2251@outlook.com+86 137 0236 4439

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026