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Effect of transcutaneous electrical acupoint stimulation on the pressure pain threshold after ovulation retrieval in IVF patients

Phase 1
Conditions
Infertility
Registration Number
ITMCTR2100005188
Lead Sponsor
Chengdu University of TCM
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

1. Aged from 21 to 42 years, infertility patients undergoing IVF treatment after oocyte retrieval;
2. Promoting ovulation with Gonadotropin Releasing Hormone Antagonist or Gonadotropin Releasing Hormone Agonist;
3. Intravenous anesthesia with drugs in oocyte retrieval;
4. Postoperative VAS 4>= points;
5. Patients are conscious, able to complete the study and sign informed consent;
6. Not participating in other ongoing clinical studies.

Exclusion Criteria

1. No acupuncture treatment in recent 3 months;
2. Patients with Chronic pain history;
3. History of long-term use of opioids, addiction to narcotic drugs, and alcohol abuse;
4. Neuropathy, mental illness or mental retardation do not correctly describe your feelings or understand visual analogue scale;
5. Allergy to the electrode, or scar, skin damage, infection, redness, swelling, violet and other manifestations at the measuring point or stimulation site;
6. Pacemaker or other implantable medical electronic devices;
7. Combined use of high frequency surgical equipment, artificial heart and lung, medical short wave, microwave therapeutic apparatus;
8. Patients with history of heart, brain, liver and kidney diseases.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analogue Scale;
Secondary Outcome Measures
NameTimeMethod
Pressure-pain Threshold;Postoperative nausea and vomiting;
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