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Space-time acupuncture for low back pain due to lumbar disc herniation: a randomized controlled trial

A clinical research of space-time acupuncture for lumbar disc herniation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17012893
Enrollment
Unknown
Registered
2017-10-06
Start date
2017-10-30
Completion date
Unknown
Last updated
2017-10-16

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

Conditions

protrusion of lumbar intervertebral disc

Interventions

Sponsors

Yunnan University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Mild and poderate low back pain with or without sciatica corresponding to herniated lumbar disc diagnosis standards formulated by North American Spine Society in 2012, and lumbar disc herniation including wnclosed, protruding, protruding showed by CT or MRI; (2) Aged 18-65 years male and female; (3) No pain medication in 2 weeks; (4) Who sign or direct relatives to sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Other low back pain was not resulted by protrusion of lumbar intervertebral disc, like fracture, prevertebral movement, surgery, cancer, infection. (2) Protrusion of intervertebral disc with large, central, free type,or with the symptom horsetail syndrome or foot droop, and whic need to surgery. (3) Lumbar disc herniation but has been performed an operation; (4) Patients with serious primary diseases of the heart, brain, blood vessels, kidneys, liver, digestive, hematopoietic disorders, diabetes, etc.; (5) Women who have fertility requirements during pregnancy, lactation and nearly half a year; (6) Failing to understand or record the relevant scoring indicators; (7) Mentally ill persons with mental retardation, moderate or higher levels of anxiety and depression; (8) Unable to cooperate with the acupuncture; (9) Who is involved in other pain medications or physical therapists, or are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
visual analogue scale(VAS) of low back and leg pain;

Secondary

MeasureTime frame
lumbar vertebra Japanese Orthopaedic Association(JOA) rating scale;Lumbar dysfunction questionnaire (Roland - Morris);Quality of life scale (sf-36);Zung self-rating anxiety scale (SAS);Zung self-rating depression scale (SDS);patient global impression of change(PGIC);

Countries

China

Contacts

Public ContactChen Zukun

Yunnan University of TCM

535362396@qq.com+86 13888768863

Outcome results

None listed

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