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

Phase 1

Recruiting

• Conditions: After-pains

• Registration Number: ITMCTR2100004513
• Lead Sponsor: The First Affiliated Hospital of Wenzhou Medical University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: Not specified

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.

Study & Design

• Study Type: Interventional study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
pain score;postpartum hemorrhage;Pain relief degree;

Secondary Outcome Measures

Name	Time	Method
Satisfaction with analgesia;Compliance evaluation;safety evaluation;