ClinicalTrials.Veeva

Menu

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

H

Huazhong University of Science and Technology

Status

Unknown

Conditions

Supervision of Pregnancy Resulting From In-vitro Fertilization

Treatments

Device: transcutaneous electrical acupoint stimulation (TEAS);EA

Study type

Interventional

Funder types

Other

Identifiers

NCT01608048
CZheng2012QN180

Details and patient eligibility

About

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

Enrollment

384 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

384 participants in 3 patient groups

control
No Intervention group
TEAS
Experimental group
Treatment:
Device: transcutaneous electrical acupoint stimulation (TEAS);EA
EA:electro-acupuncture
Experimental group
Treatment:
Device: transcutaneous electrical acupoint stimulation (TEAS);EA

Trial contacts and locations

1

Loading...

Central trial contact

Cui Hong Zheng, Doctor

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems