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Clinical Study of Eight Section Brocade Combined with Zhuijianpan Decoction for Lumbar Disc Herniation: a Randomized Controlled Trial.

Clinical study of Eight Section Brocade combined with Zhuijianpan Decoction for Lumbar Disc Herniation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034428
Enrollment
Unknown
Registered
2020-07-05
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

lumbar disc herniation

Interventions

Sponsors

The Affiliated TCM Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: According to the diagnostic criteria of "lumbar disc herniation" edited by Hu Yougu 1. Lumbago and lower extremity pain was typical of lumbosacral nerve root distribution, and the lower limb pain was more severe than low back pain; 2. There were muscle atrophy, muscle strength weakening and abnormal sensation or reflex according to the innervated area; 3. Straight leg raising test or femoral nerve stretch test was positive; 4. The imaging examination was consistent with the clinical manifestations. 1.2.2 inclusion criteria 1. 30-80 years old, regardless of gender; 2. The diagnostic criteria were met; 3. Be able to meet the test requirements; 4. The subjects were informed and agreed to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiovascular and cerebrovascular diseases, mental disorders, pregnant or lactating women; 2. Patients with traumatic lumbar disease and lumbar tumor, severe lumbar deformity, spondylolisthesis and instability; 3. Those who are allergic to or suspected to be allergic to all drugs involved in this test; 4. The patients with severe illness need surgical treatment; 5. Three months before admission, they had participated in other clinical trials.

Design outcomes

Primary

MeasureTime frame
pain intensity;lumbar function (JOA);

Secondary

MeasureTime frame
judgment standard for clinical effect;

Countries

China

Contacts

Public ContactYingfeng Cai

The Affiliated TCM Hospital of Guangzhou Medical University

caiyingfeng0101@163.com+86 13826228049

Outcome results

None listed

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