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Completed

NCT Number: NCT02644746

Efficacy and Safety of Acupuncture for Degenerative Lumbar Spinal Stenosis

Degenerative Lumbar spinal stenosis (DLSS) is a major problem for public health and the primary reason the older seek lumbar spine surgery. Acupuncture is safe and maybe effective for DLSS but the evidence is poor. Therefore, an objective assessment of acupuncture efficacy is critical for making informed decisions about its appropriate role for patients. A total of 80 participants meet prior inclusion criteria will be recruited. The participants will be allocated to acupuncture group or placebo needle (unpenetrated acupuncture) group randomly. Twenty-four treatments will be provided over 8 weeks. The primary change of Modified Roland-Morris Disability Questionnaire (RMDQ) and secondary outcomes including the change of Number Rating Scale (NRS); the change of Self-paced Walking test (SPWT); the change of Swiss Spinal Stenosis Questionnaire (SSSQ); the expectations that acupuncture might help participants with DLSS. All outcomes will be assessed at baseline, and/or after 4, 8, 20 and 32 weeks. Statistical analysis will include independent sample t-test, Chi-squared test and non-parametric test. The investigators hope the result of this trial will clarify the value of acupuncture for DLSS and help clinicians make proper decisions.

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Key information

Conditions

Degenerative Lumbar Spinal Stenosis

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Guang'anmen Hospital, China Academy of Chinese Medical Science

Beijing, Beijing Municipality, 100053, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Participants who meet all of the following conditions will be considered for enrollment. The inclusion criteria are as follows:

  • Pain in the low back, buttock, and/or lower extremity with standing, walking and/or spinal extension. (Using NRS questionnaire to measure pain symptoms, and pain measured by NRS ≥ 4.)
  • Roland-Morris score of at least 7.
  • Mild-moderate-severe lumbar central canal spinal stenosis identified by MRI or CT scan.
  • Lower extremity symptoms consistent with neurogenic claudication.
  • Age 50 to 80 years old.
  • Signed the consent and take part in this trial of his/her willing.

Exclusion criteria

  • Congenital stenosis of vertebral canal, serious indications of DLSS (such as segmental muscular atrophy, bowel and bladder disturbances), spinal nerve root canal stenosis, lumbar spondylolysis, lumbar tuberculosis, lumbar vertebral tumors, and vertebral body compression fracture.
  • Spinal instability requiring surgery.
  • Severe vascular, pulmonary or coronary artery disease that limits ambulation including recent myocardial infarction.
  • Participants who have cognitive impairment that may render the subject unable to give informed consent or provide accurate data.
  • Clinical co-morbidities that could interfere with the collection of data concerning pain and function.
  • Acupuncture within the past 30 days.
  • Administered pain control drugs during the week prior to the baseline assessment (e.g.,non-steroidal anti-inflammatory drugs or herbal anti-inflammatory agents).

Treatment and study plan

acupuncture

Device

Shenshu (BL23), Dachangshu (BL25), Weizhong (BL40), Chengshan (BL57), Taixi (KI3) acupoints will be used. For bilateral Dachangshu (BL 25), the needle will be inserted vertically at approximately 40-70 mm until participants got a electric shock feeling downward to calves, then the needle should be elevated up 2 mm, without rotating or lifting. For other four acupoints (BL23, BL40, BL57, KI3), they will be inserted 10 to 15 mm in depth with three times light amplitude rotation and lift to induce a sensation of soreness. The manipulations will be performed 3 times in total during 1 session (every 10 min). There are 24 treatment sessions after baseline, 3 times a week, and the patients will undergo a 30-min treatment each session.

placebo needle

Device

Acupuncturists will use blunt tip needles (Huatuo, Suzhou, China) that cannot penetrate skin and stimulate deep tissues, and the thrusting and twisting motions will be used by acupuncturists to simulate the treatment and blind the patients. Each placebo needle consists of four parts: needle handle, needle body, blunt tip and adhesive pad. The chosen of acupoints, treatment duration, and frequency of sessions will be the same as the acupuncture group. To guarantee blinding, the investigators will make appointments with each participant on alternate days to prevent crosstalk among groups.

Primary outcomes

  1. The change of Modified Roland-Morris Disability Questionnaire (RMDQ) from baseline.

    Time frame: Baseline, week 1-4, week 5-8, week 9-20, week 21-32

Secondary outcomes

  1. The change of Number Rating Scale (NRS) from baseline.

    Time frame: Baseline, week1-8, week 9-20, week 21-32

  2. The change of Self-paced Walking test (SPWT) from baseline to week 8.

    Time frame: Baseline, week 8.

  3. The change of Swiss Spinal Stenosis Questionnaire (SSSQ) from baseline.

    Time frame: Baseline, week 1-4, week 5-8, week 9-20, week 21-32

  4. The expectations that acupuncture might help patients DLSS will be recorded at baseline (scale).

    Time frame: Baseline.

    This expectation scale include four items, including belief "Do you think acupuncture can work?", expectation "Do you think acupuncture may help your "DLSS", preference 1"Which treatment do you prefer?", and preference2 "Did you get your treatment preference?" In fact, this is partial domain of "participants baseline information", which will be recorded at baseline. The investigators want to explore the relationship between expectation degree and primary outcome via linear regression.

Sponsors and collaborators

Lead sponsor

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Other

Registry information

Official study title

Efficacy and Safety of Acupuncture for Degenerative Lumbar Spinal Stenosis: Protocol for a Randomized Placebo-controlled Trial

Important dates

Study start
2016
Primary completion
2017
Study completion
2018
First posted
Jan 1, 2016
Registry last updated
Feb 15, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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