Suture Embedding Acupuncture for Chronic Low Back Pain

NCT ID: NCT03685864

Last Updated: 2024-04-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 51 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-10-12
• Study Completion Date: 2023-12-13

Brief Summary

Chronic low back pain (cLBP) is a common public health issue, and it is one of the main causes of disability among adults of working age. Suture embedding acupuncture is one of the most often used interventions for the treatments of cLBP. The investigators will investigate the efficacy and safety of suture embedding acupuncture for cLBP in this single center, parallel, randomized, sham-controlled clinical trial.

Detailed Description

Suture embedding acupuncture is one of the most often used interventions for the treatments of chronic low back pain (cLBP). The investigators will investigate the efficacy and safety of suture embedding acupuncture for cLBP in this single center, parallel, randomized, sham-controlled clinical trial.

Participants will be randomized into 2 groups (real acupuncture and sham acupuncture) by central allocation. Randomized participants will complete a questionnaire that solicited information regarding age, sex, marital status, occupation, education, and medical history. The blinding credibility of the treatments will be evaluated at the end of the treatment.

Real Suture embedding Acupuncture for Treatment Group To make the real suture embedding acupuncture treatment reflect an ordinary clinical practice condition, participants received standardized acupuncture treatment. That treatment was accomplished by selecting a group of acupuncture points that predefined. Acupuncture points will be bladder meridian pattern acupuncture points including Shenshu (BL23), Qihaishu (BL24), Dachangshu (BL25), and Yimmen (BL37). Treatment will be given using sterile, disposable stainless steel 23G or 25G injection needles with 1 mm 5.0 Vicryl suture inside the needle. The needles will be inserted perpendicular to a depth of 5 to 35 mm depending on the acupuncture point, which was followed by manual stimulation by bidirectional rotation to induce Deqi sensation. Deqi was defined as a dull, localized, and aching sensation, which signaled the attainment of qi. After the Deqi sensation being achieved, the suture will be embedded with a sterile stainless steel needle. After needle removal, a 5mm × 5 mm sterile tape will be adhered to the needle hole. Patients will be asked not to remove the tape unless necessary.

Sham Acupuncture for Control Group Treatment will be given using sterile, disposable stainless steel 30G or 32G acupuncture needles. The acupuncture points will be the same as real suture embedding acupuncture group. The needles will be inserted perpendicular to a depth of 5 to 35 mm depending on the acupuncture point and will be pulled up immediately. After sham acupuncture, the point will be adhered a sterile tape as real group. Patients will be asked not to remove the tape unless necessary.

Outcome Measures Primary Outcome Measure The primary outcome measure is VAS for LBP. To understand the impact of cLBP on the participants' life, VAS for bothersomeness is chosen instead of pain intensity. The participants will be asked to mark, on a 10 cm VAS (0, absence of bothersomeness; 10, the worst bothersomeness imaginable), the average degree of bothersomeness due to LBP experienced within the most recent 1 week from the day of the assessment. This measurement has substantial validity. Bothersomeness of LBP will be measured at baseline, 2-, 4-, 8-, 12-, 16-, 20-, and 24-week. The primary endpoint is the 8-week follow-up (i.e., 4 wk after finishing all of the treatments).

Secondary Outcome Measures VAS for pain intensity is a simple method evaluating the subjective intensity of pain. Pain intensity will be measured in the same way as VAS for bothersomeness. Validity of its reliability has been demonstrated. The Chinese version Oswestry Disability Index (ODI) is used to measure back pain-related dysfunction. Health-related quality of life will be measured using the well-validated EuroQol 5 dimensions (EQ-5D). A higher score is indicative of a better general health status. Participants satisfaction will be evaluated with 5 point scale (1 is worst, and 5 is best)

Statistical Analyses To determine appropriate sample size, the VAS mean difference between the 2 groups will be assumed to be 1.5 and standard deviation to be 2.73 cm with significance level([alpha]) = 0.05 and power(1-ß) = 0.80. For the equal allocation for the 2 groups, total sample size considering dropout rate of 20% will be calculated as 130 subjects, which means that at least 104 subjects would finally be required after drop outs. The investigators performed the Shapiro-Wilk normality test to determine whether or not the sample values followed a normal distribution and finally assumed normality according to the test result. For all statistical analysis, SPSS 18.0 (SPSS Inc., Chicago, IL) will be used. Significance level will be set at P < 0.05. Per protocol (PP) analysis included all participants randomized and followed up until the last follow-up point.

Conditions

Low Back Pain

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Suture Embedding Acupuncture

Suture Embedding Acupuncture 1 time for two weeks, total 3 times.

Group Type: EXPERIMENTAL

Suture Embedding Acupuncture

Intervention Type: OTHER

Suture Embedding Acupuncture at 8 acupoints (both sides of BL23, BL24, BL25, BL37). Receiving intervention 1 time in 2 weeks, and total receive 3 times.

Sham acupuncture

Sham Acupuncture 1 time for two weeks, total 3 times.

Group Type: SHAM_COMPARATOR

Sham Acupuncture

Intervention Type: OTHER

Sham Acupuncture at 8 acupoints (both sides of BL23, BL24, BL25, BL37). Receiving intervention 1 time in 2 weeks, and total receive 3 times.

Interventions

Suture Embedding Acupuncture

Suture Embedding Acupuncture at 8 acupoints (both sides of BL23, BL24, BL25, BL37). Receiving intervention 1 time in 2 weeks, and total receive 3 times.

Intervention Type: OTHER

Sham Acupuncture

Sham Acupuncture at 8 acupoints (both sides of BL23, BL24, BL25, BL37). Receiving intervention 1 time in 2 weeks, and total receive 3 times.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• cLBP lasting for at least the last 3 months.
• 10-cm visual analogue scale (VAS) for bothersomeness of LBP exceeding 4.
• Nonspecific and uncomplicated LBP that was intact on neurological examination.

Exclusion Criteria

• Pain mainly below the knee; serious spinal disorders including malignancy, vertebral fracture, spinal infection, inflammatory spondylitis and cauda equine compression; history of previous spinal surgery or scheduled surgery to address a chronic disease that could interfere with treatment effects (e.g., cardiovascular disease, diabetic neuropathy, fibromyalgia, rheumatoid arthritis, dementia, and epilepsy);
• Acupuncture treatment of LBP during the previous month
• Conditions that could compromise the safety of acupuncture (e.g., clotting disorders, taking anticoagulant agent, pregnancy, and seizure disorders);
• Severe psychiatric or psychological disorder
• Use of corticosteroids, narcotics or herbal medicine to treat LBP within one month.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Taipei Medical University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Meng-Huang Wu

Attending physician, Department of Orthopedics

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Chien-Huang Lin, PhD

Role: STUDY_CHAIR

Taipei Medical University

Locations

Taipei medical university hospital

Taipei, , Taiwan

Countries

Taiwan

References

Fan Z. Observation on 105 cases of duodenal bulbar ulcer treated by combined therapy of catgut embedding and Chinese drugs. J Tradit Chin Med. 2001 Jun;21(2):111-5. No abstract available.

Reference Type: BACKGROUND

PMID: 11498898 (View on PubMed)

Cho YJ, Song YK, Cha YY, Shin BC, Shin IH, Park HJ, Lee HS, Kim KW, Cho JH, Chung WS, Lee JH, Song MY. Acupuncture for chronic low back pain: a multicenter, randomized, patient-assessor blind, sham-controlled clinical trial. Spine (Phila Pa 1976). 2013 Apr 1;38(7):549-57. doi: 10.1097/BRS.0b013e318275e601.

Reference Type: BACKGROUND

PMID: 23026870 (View on PubMed)

Manheimer E, White A, Berman B, Forys K, Ernst E. Meta-analysis: acupuncture for low back pain. Ann Intern Med. 2005 Apr 19;142(8):651-63. doi: 10.7326/0003-4819-142-8-200504190-00014.

Reference Type: BACKGROUND

PMID: 15838072 (View on PubMed)

Other Identifiers

N201807035

Identifier Type: -

Identifier Source: org_study_id