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A multicenter prospective cohort study of multitrack screw internal fixation techniques in the lumbar spine

A multicenter prospective cohort study of multitrack screw internal fixation techniques in the lumbar spine

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080407
Enrollment
Unknown
Registered
2024-01-29
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Degenerative diseases of the lumbar spine

Interventions

Group of application of multitrack screw internal fixation in lumbar L4/L5 single-segment fusion surgery:None
Group of application of pedicle screw internal fixation in lumbar L4/L5 single-segment fusion surgery:None

Sponsors

Beijing Chaoyang Hospital, Capital Medical University, Beijing, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: (a) Age = 50 years; (b) Patients meeting diagnostic criteria; (c) Undergoing posterior lumbar L4/L5 single-segment fusion surgery; (d) Patients who are able to complete relevant imaging examinations (CT, MRI, etc.); (e) Patients without obvious cardiopulmonary function abnormalities who can tolerate the surgery; (f) Informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: (a) Previous history of spinal surgery or comorbidities such as spinal infections, fractures or tumors; (b) Patients with underlying diseases that cannot tolerate surgery; (c) Patients who are unable to complete the relevant imaging examinations for preoperative and postoperative follow-up; (d) Perioperative combined respiratory (with symptoms such as coughing and sputum), urinary tract infection (with symptoms such as urinary frequency and urgency) and other systemic infections; (e)Combination of other systemic diseases such as prevalent heart disease and genetic disease; (f) Combined mental illnesses unable to cooperate with follow-up visits.

Design outcomes

Primary

MeasureTime frame
Postoperative functional recovery;

Secondary

MeasureTime frame
Postoperative Imaging Indicators;Incidence of postoperative adjacent stage lesions;Revision surgery rate;

Countries

CHNIA

Contacts

Public ContactYuzeng Liu

Beijing Chaoyang Hospital, Capital Medical University

beijingspine2010@163.com+86 138 1155 2832

Outcome results

None listed

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