PregnancyPhase 4NCT01214772
The Effect of Heparin in Treatment IVF-ET Failure
A Phase 4 study testing heparin in people with Pregnancy and Thrombophilia, run by Yazd Medical University at 1 site in Iran.
Trial summary
Embryo transfer failure is defined as ≥3 IVF-embryo transfer failures without pregnancy . In spite of transfer of 3 good quality embryos , just 20-30% of women undergoing IVF will achieve ongoing pregnancy . There are multiple factors that influence IVF-failure. Read more about this study
- Who is it for?
- Ages 19 to 35 years, women only
- Conditions the study is for
- Pregnancy, Thrombophilia
- What is being tested?
- heparin
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 86 participants
- Where
- 1 siteIran
- Study dates
- May 2009to Jun 2010
- Phase
- Phase 4
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 19 to 35 years
- Women only
- No healthy volunteers
- Adult
Who may be able to join
- Patients who were 19-35 years old
- basal FSH < 10 IU/l
- body mass index ( BMI ) < 29 Kg/m²
- presence of both ovaries
- three or more pervious IVF-ET failures
- Top-quality embryos for transfer .
Who cannot join
- Women with polycystic ovary syndrome ( PCOS)
- endometriosis
- hydrosalpinx
- chronic systemic disease( liver, renal , thyroid and thrombocytopenia ) ●Abnormal uterine cavity
- sever male factor ( azospermia )
- Patients who had contraindication for unfractionated heparin therapy .
Trial locations and contacts
1 site in 1 country.
Iran1 site
Yazd Research and Clinical Centre for Infertility
Yazd, Yazd Province, 8916877391
About this study
Official title: the Effect of Unfractionated Heparin in Treatment of IVF-ET Failure
Embryo transfer failure is defined as ≥3 IVF-embryo transfer failures without pregnancy . In spite of transfer of 3 good quality embryos , just 20-30% of women undergoing IVF will achieve ongoing pregnancy . There are multiple factors that influence IVF-failure.
Autoantibodies may be one of the possible causes of IVF-failure , especially in unexplained and mechanical infertility .
Read more
In some studies , antiphospholipid antibody is considered as causative factor on implantation and embryo failure. However some investigators showed that combination therapy with heparin/aspirin in women with positive antiphospholipid antibody is not effective in improving of IVF-outcome . In prospective studies were not confirmed association between antiphospholipid antibody abnormalities and IVF-failure.
Recently has been relationship between thrombophilia and IVF and implantation failure.
The effect of unfractionated heparin in assisted reproductive technology (ART) cycles is prevention of thrombosis in implantation site . Although its effect is not restricted to anticoagulation and also can modulate apposition , adhesion , and penetration of embryo . Other advantages are decreasing thrombophilic risk in COH ( controlled ovarian hyperstimulation) cycles with administration of gonadotrophins . So heparin make better pregnancy rate in repeated IVF-ET failures.
There are few studies in regard to heparin effects on IVF cycles outcome . The purpose of this study is evaluation of unfractionated heparin effects on improvement of ART outcome .
This study was a prospective randomized controlled trial to assess whether administration of heparin would increased pregnancy rates in women with repeated ET-IVF failures.
Read the detailed description
Introduction Embryo transfer failure is defined as ≥3 IVF-embryo transfer failures without pregnancy . In spite of transfer of 3 good quality embryos , just 20-30% of women undergoing IVF will achieve ongoing pregnancy . There are multiple factors that influence IVF-failure.
Autoantibodies may be one of the possible causes of IVF-failure , especially in unexplained and mechanical infertility .
In some studies , antiphospholipid antibody is considered as causative factor on implantation and embryo failure. However some investigators showed that combination therapy with heparin/aspirin in women with positive antiphospholipid antibody is not effective in improving of IVF-outcome . In prospective studies were not confirmed association between antiphospholipid antibody abnormalities and IVF-failure.
Recently has been relationship between thrombophilia and IVF and implantation failure.
The effect of unfractionated heparin in assisted reproductive technology (ART) cycles is prevention of thrombosis in implantation site . Although its effect is not restricted to anticoagulation and also can modulate apposition , adhesion , and penetration of embryo . Other advantages are decreasing thrombophilic risk in COH ( controlled ovarian hyperstimulation) cycles with administration of gonadotrophins . So heparin make better pregnancy rate in repeated IVF-ET failures There are few studies in regard to heparin effects on IVF cycles outcome . The purpose of this study is evaluation of unfractionated heparin effects on improvement of ART outcome .
Materials \& Methods This study was a prospective randomized controlled trial to assess whether administration of unfractionated heparin would increased implantation and pregnancy rates in women with repeated ET-IVF failures or not . The study was performed at a reproduction center affiliated to a medical university. A total 86 patients who were candidate for IVF/ICSI with a history of three or more pervious IVF-ET failures enrolled in this study . The study was approved by the ethics committee of Research and Clinical Center for Infertility affiliated to Yazd Medical University of Medical Sciences . All patients were required to sign a written consent after the provision of complete information to them .
Treatment protocol All of the patients were treated with long protocol for ovarian stimulation. For pituitary suppression down regulation , the patients were treated with daily administration of 0.5 mg buserelin subcutaneous from day 21 of previous menstrual cycle. When desensitization was occurred, as evidenced by plasma E2 levels of ≤ 50 pg/ml and the absence of ovarian cyst on transvaginal ultrasound examination , buserelin was reduced to 0.25 mg/day and continued until the day of hCG administration. The COH was initiated with recombinant FSH or HMG 150 IU/day on the day 2 of menstrual cycle. Ovarian response was monitored by serial ultrasound examinations and evaluation of serum E2 levels, and then gonadotropin doses adjustment was done as required. Urinary HCG 10000 IU was administered when ≥3 follicles more than 18 mm.
Oocyte retrieval was performed 34-36 hours after hCG injection and IVF or ICSI was performed.
one to three top-quality embryos were transferred 48 hours after oocyte retrieval under ultrasound guidance , with a CCD embryo transfer catheter. At the same time , patients (n=86) were randomized to two groups using a computer-generated randomization . Group A ( n=43) included the patients who received unfractionated heparin 5000 IU twice a day subcutaneous injection . Treatment was started from the day of embryo transfer until 14 days after ET . If β-hCG was positive , the unfractionated heparin was continued until 6 weeks postpartum . Group B ( n=43 ) did not receive any antithrombotic drugs.
Luteal phase support was started with administration of progesterone 100 mg daily intramuscular on the day of oocyte retrieval in two groups and continued until the documentation of fetal heart activity on ultrasound.
- Conditions
- Pregnancy, Thrombophilia
- Being tested
- heparin
- Keywords
- pregnancy, heparin, fertilization
- Medical subject headings
- Thrombophilia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
heparinDrug
5000 IU subcutaneously in the day of embryo transfer until 6 week after delivery
| Study group | Role | What they receive |
|---|---|---|
| heparin,pregnancy,IVF failure | Experimental | Women in the heparin arm are administered 5000 IU twice a day on the day of embryo transfer Receives: Drug: heparin |
What is being measured
The primary outcome is the main question the study is designed to answer.
chemical pregnancy rate
Measured: until 12th gestational week
Secondary outcomes (1)
clinical pregnancy rate
Measured: until 12 gastational week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Oct 2010 (estimated)
- Study startMay 2009
- Primary completionSep 2009
- Study completionJun 2010
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for PregnancyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Investigator
- Enrolment
- 86 participants (actual)
Sponsor and investigators
- Lead sponsor
- Yazd Medical University
- Sponsor type
- University, hospital or other
- Collaborators
- Yazd Research & Clinical Center for Infertility
- Investigators
- Mehri Mashayekhy, infertility fellowship, Principal investigator, Yazd Research and Clinical Centre for Infertility
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01214772
- Sponsor's protocol ID
- 1378
- Status last verified
- Oct 2010
- First submitted
- 28 Sep 2010
- Last updated
- 5 Oct 2010
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 5 Oct 2010. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- the Effect of Unfractionated Heparin in Treatment of IVF-ET Failure
- ClinicalTrials.gov ID
- NCT01214772
- Acronym / sponsor ID
- 1378
- Conditions
- Pregnancy, Thrombophilia
- Keywords
- pregnancy, heparin, fertilization
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 86 participants (actual)
- Lead sponsor
- Yazd Medical UniversityUniversity, hospital or other
- Collaborators
- Yazd Research & Clinical Center for Infertility
- Study start
- May 2009
- Primary completion
- Sep 2009 (actual)
- Study completion
- Jun 2010 (actual)
- First posted
- 5 Oct 2010 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Embryo transfer failure is defined as ≥3 IVF-embryo transfer failures without pregnancy . In spite of transfer of 3 good quality embryos , just 20-30% of women undergoing IVF will achieve ongoing pregnancy . There are multiple factors that influence IVF-failure.
Autoantibodies may be one of the possible causes of IVF-failure , especially in unexplained and mechanical infertility .
In some studies , antiphospholipid antibody is considered as causative factor on implantation and embryo failure. However some investigators showed that combination therapy with heparin/aspirin in women with positive antiphospholipid antibody is not effective in improving of IVF-outcome . In prospective studies were not confirmed association between antiphospholipid antibody abnormalities and IVF-failure.
Recently has been relationship between thrombophilia and IVF and implantation failure.
The effect of unfractionated heparin in assisted reproductive technology (ART) cycles is prevention of thrombosis in implantation site . Although its effect is not restricted to anticoagulation and also can modulate apposition , adhesion , and penetration of embryo . Other advantages are decreasing thrombophilic risk in COH ( controlled ovarian hyperstimulation) cycles with administration of gonadotrophins . So heparin make better pregnancy rate in repeated IVF-ET failures.
There are few studies in regard to heparin effects on IVF cycles outcome . The purpose of this study is evaluation of unfractionated heparin effects on improvement of ART outcome .
This study was a prospective randomized controlled trial to assess whether administration of heparin would increased pregnancy rates in women with repeated ET-IVF failures.
Detailed description
Introduction Embryo transfer failure is defined as ≥3 IVF-embryo transfer failures without pregnancy . In spite of transfer of 3 good quality embryos , just 20-30% of women undergoing IVF will achieve ongoing pregnancy . There are multiple factors that influence IVF-failure.
Autoantibodies may be one of the possible causes of IVF-failure , especially in unexplained and mechanical infertility .
In some studies , antiphospholipid antibody is considered as causative factor on implantation and embryo failure. However some investigators showed that combination therapy with heparin/aspirin in women with positive antiphospholipid antibody is not effective in improving of IVF-outcome . In prospective studies were not confirmed association between antiphospholipid antibody abnormalities and IVF-failure.
Recently has been relationship between thrombophilia and IVF and implantation failure.
The effect of unfractionated heparin in assisted reproductive technology (ART) cycles is prevention of thrombosis in implantation site . Although its effect is not restricted to anticoagulation and also can modulate apposition , adhesion , and penetration of embryo . Other advantages are decreasing thrombophilic risk in COH ( controlled ovarian hyperstimulation) cycles with administration of gonadotrophins . So heparin make better pregnancy rate in repeated IVF-ET failures There are few studies in regard to heparin effects on IVF cycles outcome . The purpose of this study is evaluation of unfractionated heparin effects on improvement of ART outcome .
Materials \& Methods This study was a prospective randomized controlled trial to assess whether administration of unfractionated heparin would increased implantation and pregnancy rates in women with repeated ET-IVF failures or not . The study was performed at a reproduction center affiliated to a medical university. A total 86 patients who were candidate for IVF/ICSI with a history of three or more pervious IVF-ET failures enrolled in this study . The study was approved by the ethics committee of Research and Clinical Center for Infertility affiliated to Yazd Medical University of Medical Sciences . All patients were required to sign a written consent after the provision of complete information to them .
Treatment protocol All of the patients were treated with long protocol for ovarian stimulation. For pituitary suppression down regulation , the patients were treated with daily administration of 0.5 mg buserelin subcutaneous from day 21 of previous menstrual cycle. When desensitization was occurred, as evidenced by plasma E2 levels of ≤ 50 pg/ml and the absence of ovarian cyst on transvaginal ultrasound examination , buserelin was reduced to 0.25 mg/day and continued until the day of hCG administration. The COH was initiated with recombinant FSH or HMG 150 IU/day on the day 2 of menstrual cycle. Ovarian response was monitored by serial ultrasound examinations and evaluation of serum E2 levels, and then gonadotropin doses adjustment was done as required. Urinary HCG 10000 IU was administered when ≥3 follicles more than 18 mm.
Oocyte retrieval was performed 34-36 hours after hCG injection and IVF or ICSI was performed.
one to three top-quality embryos were transferred 48 hours after oocyte retrieval under ultrasound guidance , with a CCD embryo transfer catheter. At the same time , patients (n=86) were randomized to two groups using a computer-generated randomization . Group A ( n=43) included the patients who received unfractionated heparin 5000 IU twice a day subcutaneous injection . Treatment was started from the day of embryo transfer until 14 days after ET . If β-hCG was positive , the unfractionated heparin was continued until 6 weeks postpartum . Group B ( n=43 ) did not receive any antithrombotic drugs.
Luteal phase support was started with administration of progesterone 100 mg daily intramuscular on the day of oocyte retrieval in two groups and continued until the documentation of fetal heart activity on ultrasound.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| heparin,pregnancy,IVF failure | Experimental | Drug: heparinWomen in the heparin arm are administered 5000 IU twice a day on the day of embryo transfer |
Who may qualify
- Ages
- 19 to 35 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (6 listed)
- Patients who were 19-35 years old
- basal FSH < 10 IU/l
- body mass index ( BMI ) < 29 Kg/m²
- presence of both ovaries
- three or more pervious IVF-ET failures
Key exclusion criteria (6 listed)
- Women with polycystic ovary syndrome ( PCOS)
- endometriosis
- hydrosalpinx
- chronic systemic disease( liver, renal , thyroid and thrombocytopenia ) ●Abnormal uterine cavity
- sever male factor ( azospermia )
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| heparin5000 IU subcutaneously in the day of embryo transfer until 6 week after delivery | Drug | heparin,pregnancy,IVF failure |
Primary outcome
chemical pregnancy rate
Time frame: until 12th gestational week
1 secondary outcome
clinical pregnancy rate
Time frame: until 12 gastational week
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Oct 2010.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mehri Mashayekhy, infertility fellowship principal investigator
Yazd Research and Clinical Centre for Infertility
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing heparin in people with Pregnancy and Thrombophilia, run by Yazd Medical University at 1 site in Iran.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 5 Oct 2010. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Iran. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
chemical pregnancy rate (time frame: until 12th gestational week). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Oct 2010.