puerperal lumbago
Conditions
Interventions
Control group:Conventional acupuncture
Treatment group:Conventional acupuncture combined with a stick needle for stiffening tendons
Sponsors
Guangdong provincial TCM hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: (1)Meet the above diagnostic criteria for postpartum low back pain; (2)Back pain occurs between 42 days and 2 years after delivery; (3) Age 20-45 years; (4)Mean NRS pain score (scale range 0-10) =3 and =8 in the past week (5)Those who do not have localized skin breakdown, edema or petechiae, and those whose abdominal cesarean section surgical scar has not healed; (6)Voluntarily participate and sign an informed consent form after a full explanation of the purpose and procedures of this clinical trial and any risks and potential adverse effects of this trial procedure.
Exclusion criteria
Exclusion criteria: Participants were excluded if they had any of the following conditions: (1) patients with lumbar spine deformity, spinal stenosis, laminar cleft, fracture, osteoporosis and other bone diseases; (2) those who participated in other experimental interventions for low back pain within 2 weeks; (3) pregnancy status or planned parenthood during the trial; (4) low back pain caused by malignant tumor, cancer pain metastasis, gynecology, gynecological surgery, organ lesions or tuberculosis; (5) patients with serious heart, lung, brain, blood system diseases and diabetes; (6) Unable to complete the basic course of treatment, poor compliance, unable to adhere to the guiding principles and difficult follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Degree of low back pain; | — |
Secondary
| Measure | Time frame |
|---|---|
| Waist function;Ability to walk;Social life function;Mental health;Patient satisfaction; | — |
Countries
China
Contacts
Public ContactJuan Chen
Guangdong provincial TCM hospital
Outcome results
None listed