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A Randomized Controlled Clinical Study for Treatment of Lumbar Intervertebral Disc Herniation by Acupotomolysis of Flavum Ligament

A Randomized Controlled Clinical Study for Treatment of Lumbar Intervertebral Disc Herniation by Acupotomolysis of Flavum Ligament

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023446
Enrollment
Unknown
Registered
2019-05-28
Start date
2019-08-01
Completion date
Unknown
Last updated
2019-06-03

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

Conditions

Lumbar Disc Herniation

Interventions

Group 1:???
Group 2:???

Sponsors

Department of Acupuncture-Moxibustion, China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Comply with diagnostic criteria of Lumbar Disc Herniation; (2) Aged 18-75 years; (3) VAS score > 4 points; (4) Voluntary signing of informed consent.

Exclusion criteria

Exclusion criteria: 1) If the treatment is not carried out according to the regulations, it is impossible to determine the efficacy or incomplete data and other factors that affect the efficacy; 2) Patients taking lumbago treatment within 2 weeks before treatment, such as analgesics or non-steroidal anti-inflammatory drugs, hormone drugs, etc.; 3) Prevent the safe participation of the experimental design and the disease that affects the study, such as myocardial infarction or stroke, congestive heart failure, severe chronic obstructive pulmonary disease, cancer, diabetes, severe systemic disease and seriousness in the past 3 months Psychosis; 4) Patients who are receiving other related treatments that may affect the observation of the effect indicators in this study; 5) A history or clinical manifestation of bleeding tendency, including the use of anticoagulants; 6) Pregnant women and lactating women; 7) Participate in other research at the same time; 8) Unable to complete the filling of various scales.

Design outcomes

Primary

MeasureTime frame
Film degree exam;Tinel sign;VAS visual simulation score;Japanese Orthopaedic Association Score;Oswestry disability index;

Countries

China

Contacts

Public ContactShiliang Li

China-Japan Friendship Hospital

zrlishiliang@163.com+86 010 84205344

Outcome results

None listed

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