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Clinical Trials/NCT01608048
NCT01608048
Unknown
Not Applicable

Transcutaneous Electrical Acupoint Stimulation to Improve Pregnancy Rates for Women Undergoing in Vitro Fertilization

Huazhong University of Science and Technology1 site in 1 country384 target enrollmentMay 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Supervision of Pregnancy Resulting From In-vitro Fertilization
Sponsor
Huazhong University of Science and Technology
Enrollment
384
Locations
1
Primary Endpoint
clinical pregnancy rate (CPR)
Last Updated
12 years ago

Overview

Brief Summary

The objective of this study is to investigate the effect of transcutaneous electrical acupoint stimulation on pregnancy rates in women undergoing in vitro fertilization.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
February 2017
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Cui Hong Zheng

assistant research fellow

Huazhong University of Science and Technology

Eligibility Criteria

Inclusion Criteria

  • (1) infertile women \< 40 years of age, undergoing a fresh IVF or intracytoplasmic sperm injection (ICSI) cycle; (2) be an appropriate candidate with the potential for a lower success rate which defined as two or more previous unsuccessful ETs (fresh or frozen); (3) are willing to sign an informed consent form, indicating that they are aware of the investigational nature of this study that is in keeping with the policies of the institution; (4) willing to return to the study site for their study visits. The reason for our inclusion criteria is that women experienced several unsuccessful OAs or ETs may easily accept randomization to this study, and for whom adding TEAS or EA may significantly improve their clinical outcomes.

Exclusion Criteria

  • (1) major medical illnesses (like stage III heart disease, severe hypertension, uncontrolled diabetes mellitus, HIV positivity, severe bleeding dyscrasias, etc.) possibly precluding IVF or pregnancy; (2) FSH more than 20 IU/L; (3) receiving donor eggs; (4) cutaneous lesion of certain acupoint area; (5) having been previously participated in this study or having undertaken acupuncture (in whatever modality) treatment for infertility.

Outcomes

Primary Outcomes

clinical pregnancy rate (CPR)

Time Frame: 1 year

Secondary Outcomes

  • Live birth rate (LBR)(2 years)

Study Sites (1)

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