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Clinical Trials/ITMCTR2100004513
ITMCTR2100004513
Recruiting
Phase 1

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

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
The First Affiliated Hospital of Wenzhou Medical University
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Female

Investigators

Eligibility 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

  • 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.

Outcomes

Primary Outcomes

Not specified

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