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Ultrasound-Guided Deep-Layered Sacral Canal Injection Targeting the Anterior Epidural Space for Failed Back Surgery Syndrome: A Clinical Study

Ultrasound-Guided Deep-Layered Sacral Canal Injection Targeting the Anterior Epidural Space for Failed Back Surgery Syndrome: A Clinical Study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121639
Enrollment
Unknown
Registered
2026-04-01
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Failed Back Surgery Syndrome

Interventions

Intervention group:Deep injection of targeted AES through the sacral canal (intervertebral foramen approach targeting the anterior epidural space)

Sponsors

Foshan Fosun Chancheng Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-80 years, both genders; 1.American Society of Anesthesiologists (ASA) Physical Status Classification: Class ?–?; 2.Body Mass Index (BMI): 18.0–30.0 kg/m^2; 3.Postoperative lumbar spinal pain.

Exclusion criteria

Exclusion criteria: 1.History of allergy to local anesthetics or contrast agents; 2.patients with comorbid mental disorders; 3.those with contraindications to sacral canal puncture (e.g., abnormal coagulation function, skin infection at the puncture site, etc.); 4.pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of complications;The diffusion range and diffusion layer of iohexol diluent;Visual Analogue Scale (VAS) Pain Scores Before and After Treatment;

Secondary

MeasureTime frame
General patient information: gender, age, height, weight, body mass index (BMI), and sacral canal anatomical parameters (s, d, L).;Grading of Iohexol Diluent Leakage Degree at Anterior/Posterior Sacral Foramina;

Countries

China

Contacts

Public ContactWu Wenlue

Foshan Fosun Chancheng Hospital

617375291@qq.com+86 758 82778736

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026