Skip to content

Research on Transformational Medicine of Wearable Dysmenorrhea Acupoint Treatment Device

Research on Transformational Medicine of Wearable Dysmenorrhea Acupoint Treatment Device

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082859
Enrollment
Unknown
Registered
2024-04-10
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysmenorrhea

Interventions

Test Group:Wearable dysmenorrhea acupoint therapy device for treatment
Control Group:Acupuncture

Sponsors

Shanghai Research Institute of Acupuncture and Meridian
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: ? Those who meet the Western medical diagnostic criteria for primary dysmenorrhea(According to the diagnostic criteria for primary dysmenorrhea established in the national textbook "Obstetrics and Gynecology" for higher education institutions, there is lower abdominal pain during menstruation after a period of regular menstruation after menarche. Basic body temperature measurements confirm that dysmenorrhea occurs during the ovulation cycle, and gynecological examinations rule out organic diseases); ? Traditional Chinese medicine syndrome differentiation belongs to Qi stagnation and blood stasis syndrome; ? Individuals aged 18-45 years old; ? Menstrual cycle pattern (28 ± 7) days; ? Not taking painkillers, sedatives, or hormone drugs within the first 2 weeks of receiving this therapy; ? Sign the informed consent form; ? The numerical rating scale (NRS) score for pain is = 4.

Exclusion criteria

Exclusion criteria: ? Breastfeeding women; ? Combined with serious life-threatening primary diseases such as endometriosis (including adenomyosis), cardiovascular, cerebrovascular, liver, kidney, and hematopoietic systems, as well as mental illness; ? Participants in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Efficiency;

Secondary

MeasureTime frame
Pain level of dysmenorrhea;Traditional Chinese Medicine Syndrome Scale;COX menstrual symptom scale;

Countries

China

Contacts

Public ContactZhang Chunyan

Shanghai Research Institute of Acupuncture and Meridian

zh_ch_yan@163.com+86 159 2106 8889

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026