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NCT06897891
A Comparative Study on Relieving Postpartum Lumbago with Fire-dragon Cupping Therapy and Acupuncture
NA trial testing Acupuncture combined with core stability training in Postpartum Low Back Pain in 84 participants. Completed in 1 October 2024.
1 September 2024
Quick facts
| Lead sponsor | Qiaohui Ye |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 84 |
| Start date | 1 April 2024 |
| Primary completion | 1 September 2024 |
| Estimated completion | 1 October 2024 |
| Sites | 1 location across China |
Drugs / interventions tested
- Acupuncture combined with core stability training
- Dragon Tank joint core stability training
Conditions studied
- Postpartum Low Back Pain — all drugs for Postpartum Low Back Pain →
- Acupuncture — all drugs for Acupuncture →
- Core Stability Training — all drugs for Core Stability Training →
- Huolong Tank — all drugs for Huolong Tank →
Sponsor
Qiaohui Ye
Who can join
Eligibility, any sex, with Postpartum Low Back Pain or Acupuncture. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Abstract: Objective To compare the effects of fire dragon pot therapy and acupuncture on low back pain, lumbar function, self-efficacy and postpartum depression in patients with postpartum low back pain. Methods From April 2024 to September 2024, 84 postpartum patients with low back pain who met the standard of sodium discharge in Hangzhou area were recruited and divided into acupuncture group (routine acupuncture + core stability training (42 cases) and Huolongcan group (42 cases) according to random number table method. Fire dragon pot + core stability training (42 cases), the two groups each intervention 30 min, once every other day, intervention 3 times. Before and after the intervention, the visual Analogue Scale (VAS) was used to evaluate the degree of low back pain, the Oswestry Disability Index (ODI) was used to evaluate the lumbar function, the pain Self-efficacy questionnaire (PSEQ) was used to evaluate the patients' confidence in effectively coping with pain, and the Edinburgh Postpartum Depression Scale (EPDS) was used to evaluate the postpartum depression. The changes of each index before and after intervention were observed.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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Related trials
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
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- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06897891 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Qiaohui Ye
- Last refreshed: 27 March 2025
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