InfertilityPhase 4NCT03220503
Effect of Endometrial Injury Before Frozen Embryo Transfer on Pregnancy Rate
A Phase 4 study testing endometrial injury in people with Infertility, run by Ain Shams Maternity Hospital at 1 site in Egypt.
Trial summary
Research Question: In women undergoing frozen embryo transfer, does routine endometrial injury before frozen embryo transfer increase clinical pregnancy rate? Research Hypothesis: (Null Hypothesis) In women undergoing frozen embryo transfer Routine endometrial injury before frozen embryo transfer does not increase… Read more about this study
- Who is it for?
- Ages Up to 40 years, women only
- Conditions the study is for
- Infertility
- What is being tested?
- endometrial injury
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 1 siteEgypt
- Study dates
- 8 Mar 2017to 1 Oct 2017
- 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 Up to 40 years
- Women only
- No healthy volunteers
- Child, Adult
Who may be able to join
- All infertile women have high quality frozen embryos.
Who cannot join
- History of endocrine disease such as: diabetes; Hyperthyroidism and Hyperprolactinemia.
- History of hysteroscopic surgery due to intrauterine adhesions.
- History of cardiovascular, renal or liver disease .
- History of stroke or myocardial infarction.
- Poor quality embryos.
- Alcohol or Substance abuse.
Trial locations and contacts
1 site in 1 country.
Egypt1 site, 1 recruiting
- Recruiting
ART unit - Ain Shams university Matrnity Hospital
Cairo
yasser sherbiny, invistgator, +201008961189, drysherbiny89@gmail.com
About this study
Research Question:
In women undergoing frozen embryo transfer, does routine endometrial injury before frozen embryo transfer increase clinical pregnancy rate?
Research Hypothesis:
(Null Hypothesis) In women undergoing frozen embryo transfer Routine endometrial injury before frozen embryo transfer does not increase clinical pregnancy rate.
(Alternative Hypothesis) In women undergoing frozen embryo transfer, endometrial injury before the transfer may increase pregnancy rate.
Read the detailed description
Suitable women will be invited to participate in the study then a signed and informed consent will be obtained from them. When the patient's consent is obtained, they are to be included into the study.
Data Collection:
During first visit, all patients will undergo complete clinical examination and detailed medical history will be obtained. Each patient will have a Case Record Form (CRF) in which the following data will be recorded.
- Patient number (according to the randomization schedule).
- Age, BMI.
- Past medical and surgical history.
- Duration of infertility.
Procedure:
Endometrial injury:
A single induced injury will be done on the posterior endometrium on day 7 of the transfer cycle by using modified Cook catheter Protocol for vitrification Embryos will first loaded with equilibrium solution containing7.5% ethylene glycol (EG) and 7.5% dimethyl sulphoxide (DSMO) (Sigma-Aldrich) for 5-10 minute at room temperature and then with vitrification solution containing 15% EG, 15% DSMO and 0.5 mol/L sucrose for 50-60 seconds at room temperature. After observed cellular shrinkage, embryos will quickly stored in liquid nitrogen (LN) for at least 2 months. At warming, embryos will removed from LN and embryos will exposed to thawing solution containing sucrose at 37°C temperature for 50-60 seconds and then embryos will sequentially incubated in diluents solutions before being transferred .
Evaluation and transfer of thawed embryos After thawing, each embryo will evaluated twice, once immediately for the number of surviving blastomeres and again after 18 hours post-thaw in vitro culture for assessing of mitosis and number of blastomeres. Embryos will considered survived if >50% of each blastomere are intact and selected for intrauterine transfer (Depending on patients' embryos, 2 or 3 embryos will transferred).
Embryos will classified as fully intact or excellent morphology (100% cells survived with <10% fragmentation) or good morphology (100% cells survived with 10%-20% fragmentation), partially damaged or poor morphology (≥50% cells survived with or without any fragmentation) and Degenerated embryos (<50% cells survived) .Only fully intact and partially damaged embryos will transferred. Degenerated or arrested embryos will not transferred.
Protocol of endometrial preparation before Frozen Embryo Transfer (FET) :
There are different protocols for FET cycles. That is true for both "natural cycle" FETs and for "hormone replacement cycle" frozen-thawed embryo transfers. We will use hormone replacement cycles because they have better success rates. However, some clinics offer a natural cycle FET approach. Success rates are higher with hormone replacement, or "controlled" FET cycles.
Medicines and Drugs in a Frozen Embryo Transfer FET Cycle
- Gonadotropin-Releasing Hormone agonist (such as Lupron) will be given, either midluteal (day 21) or overlapping with a birth control pill.
- Down-regulation will be confirmed by ultrasound and blood tests.
- Estradiol valerate 2 mg twice daily (orally) will start after the period. This dose may need to be increased after monitoring of the uterine lining thickness.
- When the endometrium has a "good" thickness( > 8 mm), progesterone will be started (intramuscular shots, or a vaginal product).
- Embryo transfer will be planned for 3-6 days later - depending on the stage of development of the embryos to be transferred.
- Estrogen and progesterone will be continued in the luteal phase.
- Pregnancy testing will be done 9-14 days after transfer - depending on the stage of development of the embryos replaced and the preferences of the fertility clinic.
- If pregnant, estrogen and progesterone will be continued until about 10-15 weeks of pregnancy and then weaned off.
- Conditions
- Infertility
- Being tested
- endometrial injury
- Medical subject headings
- Infertility
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
endometrial injuryProcedure or surgery
single induced injury will be done on the posterior endometrium on day 7 of the transfer cycle by using modified Cook catheter.
| Study group | Role | What they receive |
|---|---|---|
| Group (A) | Experimental | consists of 25 patients will receive frozen embryo with endometrial scratching on day 7 of transfer cycle. Receives: Procedure: endometrial injury |
| Group (B) | No intervention | consists of 25 patients will receive frozen embryo without endometrial scratching as control group. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Chemical pregnancy rate
serum Beta -Human Chorionic Gonadotropin positive
Measured: two weeks after frozen embryo transfer
Secondary outcomes (1)
Clinical pregnancy rate
appearance of gestational sac on trans-vaginal ultrasound
Measured: four weeks after frozen embryo transfer
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Jul 2017
- Study start8 Mar 2017
- Primary completion9 Sep 2017 (estimated)
- Study completion1 Oct 2017 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for InfertilityStudies 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
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ain Shams Maternity Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Yasser sherbiny, Ain Shams Maternity Hospital
- Investigators
- Adel Sh Salah El-Din, Ass. Prof., Study director, Ain Shams UniversityMohammed A Faris, Lecturer, Study director, Ain Shams UniversityMohamed E Shawky, Lecturer, Study director, Ain Shams University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03220503
- Sponsor's protocol ID
- AinShamsMH Ysherbiny
- Status last verified
- Jul 2017
- First submitted
- 15 Jun 2017
- Last updated
- 18 Jul 2017
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 18 Jul 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Endometrial Injury Before Frozen Embryo Transfer on Pregnancy Rate
- ClinicalTrials.gov ID
- NCT03220503
- Acronym / sponsor ID
- AinShamsMH Ysherbiny
- Conditions
- Infertility
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Ain Shams Maternity HospitalUniversity, hospital or other
- Study start
- 8 Mar 2017 (actual)
- Primary completion
- 9 Sep 2017 (estimated)
- Study completion
- 1 Oct 2017 (estimated)
- First posted
- 18 Jul 2017 (actual)
- 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.
Research Question:
In women undergoing frozen embryo transfer, does routine endometrial injury before frozen embryo transfer increase clinical pregnancy rate?
Research Hypothesis:
(Null Hypothesis) In women undergoing frozen embryo transfer Routine endometrial injury before frozen embryo transfer does not increase clinical pregnancy rate.
(Alternative Hypothesis) In women undergoing frozen embryo transfer, endometrial injury before the transfer may increase pregnancy rate.
Detailed description
Suitable women will be invited to participate in the study then a signed and informed consent will be obtained from them. When the patient's consent is obtained, they are to be included into the study.
Data Collection:
During first visit, all patients will undergo complete clinical examination and detailed medical history will be obtained. Each patient will have a Case Record Form (CRF) in which the following data will be recorded.
- Patient number (according to the randomization schedule).
- Age, BMI.
- Past medical and surgical history.
- Duration of infertility.
Procedure:
Endometrial injury:
A single induced injury will be done on the posterior endometrium on day 7 of the transfer cycle by using modified Cook catheter Protocol for vitrification Embryos will first loaded with equilibrium solution containing7.5% ethylene glycol (EG) and 7.5% dimethyl sulphoxide (DSMO) (Sigma-Aldrich) for 5-10 minute at room temperature and then with vitrification solution containing 15% EG, 15% DSMO and 0.5 mol/L sucrose for 50-60 seconds at room temperature. After observed cellular shrinkage, embryos will quickly stored in liquid nitrogen (LN) for at least 2 months. At warming, embryos will removed from LN and embryos will exposed to thawing solution containing sucrose at 37°C temperature for 50-60 seconds and then embryos will sequentially incubated in diluents solutions before being transferred .
Evaluation and transfer of thawed embryos After thawing, each embryo will evaluated twice, once immediately for the number of surviving blastomeres and again after 18 hours post-thaw in vitro culture for assessing of mitosis and number of blastomeres. Embryos will considered survived if >50% of each blastomere are intact and selected for intrauterine transfer (Depending on patients' embryos, 2 or 3 embryos will transferred).
Embryos will classified as fully intact or excellent morphology (100% cells survived with <10% fragmentation) or good morphology (100% cells survived with 10%-20% fragmentation), partially damaged or poor morphology (≥50% cells survived with or without any fragmentation) and Degenerated embryos (<50% cells survived) .Only fully intact and partially damaged embryos will transferred. Degenerated or arrested embryos will not transferred.
Protocol of endometrial preparation before Frozen Embryo Transfer (FET) :
There are different protocols for FET cycles. That is true for both "natural cycle" FETs and for "hormone replacement cycle" frozen-thawed embryo transfers. We will use hormone replacement cycles because they have better success rates. However, some clinics offer a natural cycle FET approach. Success rates are higher with hormone replacement, or "controlled" FET cycles.
Medicines and Drugs in a Frozen Embryo Transfer FET Cycle
- Gonadotropin-Releasing Hormone agonist (such as Lupron) will be given, either midluteal (day 21) or overlapping with a birth control pill.
- Down-regulation will be confirmed by ultrasound and blood tests.
- Estradiol valerate 2 mg twice daily (orally) will start after the period. This dose may need to be increased after monitoring of the uterine lining thickness.
- When the endometrium has a "good" thickness( > 8 mm), progesterone will be started (intramuscular shots, or a vaginal product).
- Embryo transfer will be planned for 3-6 days later - depending on the stage of development of the embryos to be transferred.
- Estrogen and progesterone will be continued in the luteal phase.
- Pregnancy testing will be done 9-14 days after transfer - depending on the stage of development of the embryos replaced and the preferences of the fertility clinic.
- If pregnant, estrogen and progesterone will be continued until about 10-15 weeks of pregnancy and then weaned off.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group (A) | Experimental | Procedure: endometrial injuryconsists of 25 patients will receive frozen embryo with endometrial scratching on day 7 of transfer cycle. |
| Group (B) | No intervention | –consists of 25 patients will receive frozen embryo without endometrial scratching as control group. |
Who may qualify
- Ages
- Up to 40 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (1 listed)
- All infertile women have high quality frozen embryos.
Key exclusion criteria (6 listed)
- History of endocrine disease such as: diabetes; Hyperthyroidism and Hyperprolactinemia.
- History of hysteroscopic surgery due to intrauterine adhesions.
- History of cardiovascular, renal or liver disease .
- History of stroke or myocardial infarction.
- Poor quality embryos.
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 |
|---|---|---|
| endometrial injurysingle induced injury will be done on the posterior endometrium on day 7 of the transfer cycle by using modified Cook catheter. | Procedure or surgery | Group (A) |
Primary outcome
Chemical pregnancy rate
Time frame: two weeks after frozen embryo transfer
serum Beta -Human Chorionic Gonadotropin positive
1 secondary outcome
Clinical pregnancy rate
Time frame: four weeks after frozen embryo transfer
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Jul 2017.
- Individual participant dataSharing planned: Undecided
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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.
Adel Sh Salah El-Din, Ass. Prof. study director
Ain Shams University
Mohammed A Faris, Lecturer study director
Ain Shams University
Mohamed E Shawky, Lecturer study director
Ain Shams University
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 endometrial injury in people with Infertility, run by Ain Shams Maternity Hospital at 1 site in Egypt.
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 1 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: status not confirmed, as of the sponsor's last update on 18 Jul 2017. 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 Egypt. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Yasser Sherbiny, invistgator (+201008961189, drysherbiny89@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Chemical pregnancy rate (time frame: two weeks after frozen embryo transfer). 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 18 Jul 2017; AzTrials last refreshed its copy on 8 Nov 2026.