Wet Cupping (AlHijamah); Double Versus Single Cupping Technique

National Center for Complementary and Alternative Medicine, Saudi Arabia

Status

Completed

Conditions

Low Back Pain

Treatments

Procedure: wet cupping

Study type

Interventional

Funder types

Other

Identifiers

NCT02631382

NCCAM - TRIAL - CUPPING2

Details and patient eligibility

About

Randomized clinical trial to compare the effectiveness and safety of double (traditional) versus single (Asian) cupping techniques in chronic low back pain.

Full description

Chronic Low Back Pain is a very common pain disorder in the primary care. As in many chronic pain conditions, patients are usually asking for alternative options, especially local traditional and therapies including wet cupping, to replace the long-term use of painkillers. The majority of the wet cupping trials conducted abroad used different techniques, which is different from our local traditional wet cupping technique. This study can identify the technique that is more efficacious in reducing pain, prolonging the pain relieve period, and decrease patient dependence on painkillers in chronic low back pain.The aim of this study is to compare the effectiveness and safety of double (traditional) versus single (Asian) cupping techniques in chronic low back pain. This a randomized comparative effectiveness pilot clinical trial. After taking written informed consent, patient with chronic low back pain will be randomized into two groups, one group to receive wet cupping therapy with the Traditional double technique, the other group to receive it with the Asian single technique. Numeric Rating Scale, Present Pain Intensity and Oswestry Disability Questionnaire will be used to measure the outcome before and after the intervention, one week after the intervention, then two weeks after. Wilcoxon rank sum test for the continuous dependent data analysis and the analysis of covariance ANCOVA, to compare both groups mean scores will be used. The outcome baseline for each score will be used as the covariate. Chi square or Fisher's exact test will be used to compare categorical data with Minimal Clinical Improvement Difference within and between the two groups.

Enrollment

70 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male and Female
Age equal or more than 18 years up to 60 years
Chronic low back pain (at least the duration ≥ 3 months)
Not on anti-inflammatory or pain killers for the last 15 days.

Exclusion criteria

Patients received wet-cupping therapy before in the last three months
Patients who have low back pain due to specific and known etiological causes (infection, tumor, osteoporosis, ankylosing spondylitis, fracture, inflammatory process, radicular syndrome, and cauda equinal syndrome)
Patients who are inappropriate to the wet cupping treatment (AIDS, Hepatitis, Tuberculosis, Syphilis. The referring physicians will be advised to exclude those patients)
Patients currently receiving any anticoagulant, antiplatelet medications
Anemia, thrombocytopenia, Coagulopathy or Hemorrhagic disease like hemophilia
Had undergone a surgery, or had bleeding injury, or had blood donation
Uncontrolled hypertension, Ischemic heart disease, previous transient ischemic attack or stroke
Diabetes, known renal and / or hepatic diseases
Patients who are in pregnancy or have plan to conception
Previously or currently drug addicts
Any other severe disease or disabling medical condition