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Clinical Study on the Efficacy of Transcutaneous Electrical Acupoint Stimulation in the Treatment of Postpartum Uterine Contraction Pain

A study of the transcutaneous electrical acupoint stimulation on postpartum uterine contractive pain and related problems

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043825
Enrollment
Unknown
Registered
2021-03-04
Start date
2021-03-04
Completion date
Unknown
Last updated
2021-07-05

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

Conditions

After-pains

Interventions

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 43 Years

Inclusion criteria

Inclusion criteria: 1. 1-2 days postpartum, aged 18-43 years; Gestational age was 37-42 weeks; Never received acupuncture therapy; The pain of uterine contraction was graded by NRs. The pain index was divided into four grades: 0-10 for different degrees of pain, (NRS) score >= 4 for the first time; 2. Subjects with normal blood routine, heart, liver and kidney function; 3. Conscious subjects can recognize and understand Chinese and complete the evaluation scale; No mental illness; 4. The subjects without intellectual and mental disorders have normal language expression ability, have the ability to judge their own pain and general conditions, and can cooperate to evaluate the content of pain and quality of life. 5. Informed consent signed by the patient or his relatives.

Exclusion criteria

Exclusion criteria: 1. Patients with heart, liver, lung, kidney and hematopoietic system diseases; 2. Subjects with pregnancy complications or complications; 3. Subjects with mental disorder, hemiplegia or sensory disturbance of lower limbs; 4. Subjects using other drugs, physical therapy or non drug analgesia.

Design outcomes

Primary

MeasureTime frame
pain score;Pain relief degree;postpartum hemorrhage;

Secondary

MeasureTime frame
Satisfaction with analgesia;safety evaluation;Compliance evaluation;

Countries

China

Contacts

Public ContactCong Wenjie

The First Affiliated Hospital of Wenzhou Medical University

38789081@qq.com+86 13567780639

Outcome results

None listed

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