AzTrials
AzTrials

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.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

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.

Yasser Sherbiny, invistgator contact

+201008961189

drysherbiny89@gmail.com

Egypt1 site, 1 recruiting
  • ART unit - Ain Shams university Matrnity Hospital

    Cairo

    yasser sherbiny, invistgator, +201008961189, drysherbiny89@gmail.com

    Recruiting

Other trials in Egypt

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

  1. Gonadotropin-Releasing Hormone agonist (such as Lupron) will be given, either midluteal (day 21) or overlapping with a birth control pill.
  2. Down-regulation will be confirmed by ultrasound and blood tests.
  3. 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.
  4. When the endometrium has a "good" thickness( > 8 mm), progesterone will be started (intramuscular shots, or a vaginal product).
  5. Embryo transfer will be planned for 3-6 days later - depending on the stage of development of the embryos to be transferred.
  6. Estrogen and progesterone will be continued in the luteal phase.
  7. 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.
  8. 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 groups in NCT03220503
Study groupRoleWhat they receive
Group (A)Experimentalconsists of 25 patients will receive frozen embryo with endometrial scratching on day 7 of transfer cycle.
Receives: Procedure: endometrial injury
Group (B)No interventionconsists 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.

  1. Chemical pregnancy rate

    serum Beta -Human Chorionic Gonadotropin positive

    Measured: two weeks after frozen embryo transfer

Secondary outcomes (1)
  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.

  1. First posted18 Jul 2017
  2. Study start8 Mar 2017
  3. Primary completion9 Sep 2017 (estimated)
  4. Study completion1 Oct 2017 (estimated)

Resources

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)
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

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in