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NCT01778621 Clinical Trial

Effect of Acupuncture on Anti Mullerian Hormone and Assisted Reproduction Outcome in PCOS Patients Undergoing IVF

PCOS Clinical Trial

Official title:
Acupuncture Treatment Versus Non-acupuncture During IVF

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01778621
Other study ID # MINA-1978
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2011
Est. completion date May 2012

Study information
Verified date July 2019
Source Huazhong University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Acupuncture at follicular phase of the cycle may improve the pregnancy rate. This study aims to compare assisted reproduction outcome between two groups of PCOS patients underwent IVF, one group received acupuncture and other group without acupuncture.

Description:

Follicular phase acupuncture applied for PCOS patients underwent IVF to evaluate the effect of acupuncture on anti-mullerian hormone (AMH) and the effect on assisted reproduction outcome. It applied at certain acupoints according to the principles of traditional Chinese medicine.

Recruitment information / eligibility
Status Completed
Enrollment 102
Est. completion date May 2012
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria::

- PCOS patients with patent one or two fallopian tubes, normal uterine cavity and partners with normal semen parameters.

- infertility

- 20-40 years

- IVF treatment -

Exclusion Criteria:

- patients with disorders that have the similar clinical presentation

- closed both tubes

- abnormal semen parameters

- intracytoplasmic sperm injection (ICSI)

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Acupuncture(Hwato®)
acupuncture using 4cm long disposable stainless steel hair-thin needles manufactured by Suzhou medical appliance factory (China).

Locations
Country Name City State
China Assisted Reproduction Center, Department of Obstetrics and Gynecology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei

Sponsors (2)
Lead Sponsor Collaborator
Amina Altutunji Huazhong University of Science and Technology

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Clinical pregnancy rate. Increase in pregnancy rate 13 months
Secondary Ongoing pregnancy rate Increase in ongoing pregnancy rate 15 months
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