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Enhanced Assisted Reproductive Technology Pregnancy Rate by Prostacyclin Analog (Iloprost)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified March 2012 by Fertility Specialists of Houston.
Recruitment status was:  Recruiting
ClinicalTrials.gov Identifier:
First Posted: March 9, 2012
Last Update Posted: October 12, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Origio A/S
Information provided by (Responsible Party):
Fertility Specialists of Houston
Human fallopian tube secretes high concentration of prostacyclin. Fallopian tube is the site for early embryo development. The effect of prostacyclin on human early embryo development is waiting to be clarified. The study hypothesis is prostacyclin can enhance early embryo development.

Condition Intervention
Pregnancy Drug: Iloprost Other: normal saline

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Pilot Study to Examine Iloprost Can Enhance Human Assisted Reproductive Technology Pregnancy Outcomes.

Resource links provided by NLM:

Further study details as provided by Fertility Specialists of Houston:

Primary Outcome Measures:
  • Presence of embryo sac in uterus under ultrasound [ Time Frame: 5 weeks after embryo transfer ]
    The competency of embryo is determined by its ability to implant into endometirum.

Secondary Outcome Measures:
  • The delivery outcome is the secondary outcome measured. [ Time Frame: 10 months after embryo transfer ]
    The live birth and the weight and length of baby is examined.

Estimated Enrollment: 100
Study Start Date: January 2010
Estimated Study Completion Date: December 2013
Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
This is the study group with 1 uM Iloprost.
Drug: Iloprost
supplement in culture medium during culture in the lab. The concentration is 1 uM.
Other Name: Ilomedin
This is the control group with vehicle (normal saline) only.
Other: normal saline
Supplement with vehicle only no Iloprost.

Detailed Description:

Huang et al, found that human fallopian tube expresses prostacyclin synthetase and cyclooxygenase. These enzyme systems synthesize abundant prostacyclin (PGI2). In the fallopian tube PGI2 causes smooth muscle relaxation, possibly facilitating tubal transport of gametes and embryos. Huang et al reported that addition of the PGI2 analogue Iloprost to embryo culture media significantly enhanced mouse embryo development to the blastocyst and complete hatched stages. The implantation and live birth rates of Iloprost cultured embryos were significantly better than non-Iloprost embryos in the mouse model. The mean weights of fetal mice were not significant different from control group. There was no teratogenic effect observed.

In a previously presented study, the investigators cultured donated frozen human zygotes in culture media with and without the addition of Iloprost. The Iloprost treated embryos showed significantly better growth rate and morphology, as determined by the size, and grading of the trophectoderm and inner cell mass.

Iloprost is FDA approved for the treatment of pulmonary hypertension. It has a significantly longer half-life than native PGI2. Iloprost is a class C pregnancy drug and has not been associated with teratogenic effects. This study intends to expand the usage of Iloprost to culture embryos.


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 39 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
ART cases with age < 40 and without pre-implantation genetic diagnosis

Inclusion Criteria:

  • ART case

Exclusion Criteria:

  • age < 40
  • no pre-implantation genetic diagnosis procedure
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01549171

United States, Texas
Fertility Specialists of Houston Recruiting
Houston, Texas, United States, 77054
Contact: Wan-Song A Wun, Ph.D.    713-512-7680    awun@obgynassociates.com   
Contact: George M Grunert, M.D.    713-512-7760    ggrunert@fshivf.com   
Sub-Investigator: Randall C Dunn, M.D.         
Sub-Investigator: Schenk M Leah, M.D.         
Sub-Investigator: Mangal K Rakesh, M.D.         
Sub-Investigator: Chauhan R Subodh, M.D.         
Sub-Investigator: Wan-Song A Wun, Ph.D.         
Sponsors and Collaborators
Fertility Specialists of Houston
Origio A/S
Principal Investigator: George M Grunert, M.D. Obstetrical & Gynecological Associates
  More Information

Responsible Party: Fertility Specialists of Houston
ClinicalTrials.gov Identifier: NCT01549171     History of Changes
Other Study ID Numbers: OGAFSH-01
First Submitted: March 6, 2012
First Posted: March 9, 2012
Last Update Posted: October 12, 2017
Last Verified: March 2012

Keywords provided by Fertility Specialists of Houston:
Human ART

Additional relevant MeSH terms:
Platelet Aggregation Inhibitors
Vasodilator Agents
Antihypertensive Agents