Skip to content

Early identification and clinical efficacy of long round needle therapy for identifying the focal points of the tendon system after minimally invasive lumbar MIDLF surgery

Early identification and clinical efficacy of long round needle therapy for identifying the focal points of the tendon system after minimally invasive lumbar MIDLF surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000417
Enrollment
Unknown
Registered
2025-02-27
Start date
2024-12-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Diseases such as lumbar disc herniation lumbar spinal stenosis lumbar spondylolisthesis degenerative lumbar deformities etc

Interventions

control group:Loxoprofen sodium was given orally for pain relief, and mecobalamin was given orally for nerve nutrition during the treatment. The patient was treated for three weeks before drug treatme
Jiejie Treatment Group:Long-round needle unknotting therapy,oral mecobalamin was used for nerve nutrition during treatment, and the patient was treated for three weeks before drug treatment was discon

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age range from 18 to 80 years old regardless of gender; 2. Patients who undergo MIDLF surgery for diseases such as lumbar disc herniation lumbar spinal stenosis lumbar spondylolisthesis degenerative lumbar deformities etc; 3. At one month follow-up after surgery patients reported residual or new onset of moderate to severe back pain with a Visual Analog Scale (VAS) greater than 3 points for back pain.

Exclusion criteria

Exclusion criteria: 1. Postoperative incision infection cerebrospinal fluid leakage poor healing or skin damage in lumbar spine surgery; 2. Loose displaced or failed internal fixation; 3. Patients with lumbar infection tumor trauma and revision surgery; 4. Patients with severe heart lung and brain diseases.

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
operation time;intraoperative blood loss;BMI;comorbidities;incision length;36-item Short-Form;therapeutic evaluation;Oswestry disability index;operative segment;main diagnosis;Age;gender;

Countries

China

Contacts

Public ContactHaolin Sun

Peking University First Hospital

sunhaolin@vip.163.com+86 136 8114 6156

Outcome results

None listed

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