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PregnancyMC_CC-TestNCT02962466

Multicenter Prospective Cumulus Cell Test Study

A study testing CC-Test in people with Pregnancy, run by Universitair Ziekenhuis Brussel at 2 sites in Belgium.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

Performing an additional non invasive oocyte diagnostic test based on cumulus gene expression could improve the outcome of the ART cycle. Read more about this study

Who is it for?
Ages Up to 40 years, women only
Conditions the study is for
Pregnancy
What is being tested?
CC-Test
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
2 sitesBelgium
Study dates
Nov 2016to Nov 2020
Phase
Interventional
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

  • scheduled for intracytoplasmatic sperm injection (ICSI) and single embryo transfer on day 3
  • patients down regulated with gonadotropin-releasing hormone (GnRH) antagonist and stimulated with Highly Purified human Menopausal Gonadotropin (HP-hMG)
  • no more than 2 previous IVF or ICSI cycles with transfer prior to this one.
  • Body mass index (BMI) should be higher than 17 and lower than 32
  • patients should have regular menstrual cycles (between 24 and 35 days).

Who cannot join

  • are smokers (>10 cigarettes per day)
  • patients requesting Prenatal Genetic Diagnosis
  • patients having polycystic ovary syndrome (PCOS), or Severe Endometriosis (AFS Stage 3-4)
  • couples where the partner has an extremely low sperm count e.g.: extreme oligo-astheno-teratozoospermia (OAT), (<100.000/ml) or testicular sperm extraction (TESE)
  • results of eventual preceding cycles may not indicate a known genetic disease, or low ovarian response or an oocyte maturation defect.

Trial locations and contacts

2 sites in 1 country.

Tom Adriaenssens, Msc. contact

+ 32 2 477 50 50

Tom.Adriaenssens@UZBrussel.be

Johan Smitz, Prof. Dr. contact

+ 32 2 477 50 50

Johan.Smitz@UZBrussel.be

Belgium2 sites, 2 recruiting
  • ULB Erasme

    Anderlecht, 1070

    Fabienne Devreker, Prof. Dr., + 32 2 555 45 77

    Noe Moutard, Dr., + 32 2 555 51 51, Noe.Moutard@erasme.ULB.ac.be

    Recruiting
  • Universitair Ziekenhuis Brussel

    Jette, Brussels Capital, 1090

    Tom Adriaenssens, Msc., + 32 2 477 50 50, Tom.Adriaenssens@UZBrussel.be

    Johan Smitz, Prof. Dr., + 32 2 477 50 50, Johan.Smitz@UZBrussel.be

    Recruiting

Other trials in Belgium

About this study

Official title: Cumulus Cell Messenger Ribonucleic Acid (mRNA) Analysis as Oocyte Quality Marker in the Fertility Lab in a Prospective Multicenter Study

Performing an additional non invasive oocyte diagnostic test based on cumulus gene expression could improve the outcome of the ART cycle.

Read the detailed description

Background:

Currently, embryo selection before embryo transfer is done on the basis of morphological characteristics only. The morphology based selection procedure has only a limited predictive value. The need of an additional oocyte/embryo evaluating method is therefore required. This method should preferentially be: non invasive, objective, and available early in development. Each oocyte is surrounded with cumulus cells, cells which are normally disposed of during the assisted reproductive technique (ART)-procedure. A diagnostic test based on the cumulus cells fits al of the required criteria. In the current study the use of an oocyte diagnostic test based on cumulus cell gene expression is evaluated.

Primary purpose:

Validate a non invasive diagnostic test, not curing the infertility condition but improving the ART-treatment and as such reducing the physical and psychological effect of the (eventually failed) ART procedure or the potential side effects of this procedure on the patients.

Quality assurance plan for Data check and Source Data Verification:

The aim, the study design, the eligible patient population, the study plan and specific requirements were discussed on several occasions at the test sites. Clear collaborative agreements were made between the partners involved in this study. These stipulate the study protocol and the required action from each party at the specific time points and communication procedures. A trial initiation meeting was conducted on site by the PI. Interim evaluations for site monitoring and validation of data registration are foreseen. These will be initiated as soon as 10 patients are included in the study and can occur with every extra 5 patients being included. Data checks and verifications are foreseen on regular basis to be done by the trained study managers from the different study centers.

Definitions:

For study patients and matched controls serum human chorionic gonadotropin (hCG) is measured on day 14-17 after pick up. If positive, the hCG is followed up at day 20 and 25 (positive beta-hCG Pregnancy). All patients with a positive hCG are further followed up: 1) to detect a development of the foetal sac with positive heartbeat in weeks 7-8 of pregnancy (Clinical Pregnancy), 2) to have a routine ultrasound evaluation at weeks 12, 20 and 32 of pregnancy, 3) to have data on delivery and child health (Live Birth). The total number of pregnancies obtained from the stimulation cycles included in the study will be referred to as the Cumulative Pregnancy for each of the study groups.

Study design and Data analysis:

The study is a prospective matched control and assessor blind study. Most of the details on the study design are already described else ware in this document. It should however be noted that the assessor performing the additional diagnosis for the oocytes using the CC-Test is blind for eventual development of the oocyte into an embryo and the quality of these embryo based on the morphology.

Sample size was assessed based on retrospective studies performed by the Follicle Biology research laboratory (FOBI) UZBrussel. These indicated that with an ongoing pregnancy rate (OPR) in the two control groups of 30-40% and an expected OPR of 50%-70% the number of participants required is 20 to distinguish the difference with a power of 80%. For this reason at least 30 informative patients will be included in each study arm for each test site.

Clinical patient data related to the inclusion and exclusion criteria should be available and evaluated by the local investigator prior to enrolment of the patient in the study. Absence of any data related to the evaluation of the ART procedure or outcome will exclude this patient from further analysis. Data inconsistency or out of range results will be considered as absent data.

The statistical analysis of the results will be performed by a professional statistician experienced with the field, terminology and endpoints, using the best fit statistical method for each endpoint. For the analysis of the primary and secondary endpoints these include amongst others: Chi-square analysis, Kaplan-Meier analysis and multiple regression analysis, based on generalized linear models.

Interim analysis:

A first evaluation will be done when 20 cases, having had transfer after the CC-Test, are completed. This will comprise data on positive beta-hCG pregnancy, clinical pregnancy (7weeks).

Conditions
Pregnancy
Being tested
CC-Test

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CC-TestOther

    classification of the oocyte based on the expression pattern observed in the cumulus cells

Study groups in NCT02962466
Study groupRoleWhat they receive
CC-Test diagnosis and Day 3 transferExperimentalPatients undergo the standard ART treatment, as prescribed by the treating physician, with standard morphology based scoring of the embryos + the extra cumulus cell based diagnosis and transfer of the best embryo based on morphology and CC diagnosis on day 3 of embryo growth (cleavage stage embryo).
Receives: Other: CC-Test
D3 transfer control groupNo interventionPatients undergo the standard ART treatment, as prescribed by the treating physician, with standard morphology based scoring of the embryos and transfer of the best embryo based on day 3 of embryo growth (cleavage stage embryo).
D5 transfer control groupNo interventionPatients undergo the standard ART treatment, as prescribed by the treating physician, with standard morphology based scoring of the embryos and transfer of the best embryo based on day 5 of embryo growth (blastocyst stage embryo).

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Clinical Pregnancy as observed by ultrasound

    this observation is routinely performed by the treating physician for every patient undergoing standard ART treatment and is thus available from the fertility center database

    Measured: 2 months after embryo transfer

Secondary outcomes (3)
  1. positive beta-hCG Pregnancy as observed by serum analysis

    this observation is routinely performed by the treating physician for every patient undergoing standard ART treatment and is thus available from the fertility center database

    Measured: 12-17 days after transfer

  2. Live Birth by questionaire

    this observation is routinely performed by the study nurses of the fertility center for every patient undergoing standard ART treatment and is thus available from the fertility center database

    Measured: et least 9 months after embryo transfer

  3. Cumulative Pregnancy

    this is the compilation of the data gathered in endpoint 1 and 3 for eventual consecutive cycles. This observation is routinely performed by the study nurses of the fertility center for every patient undergoing standard ART treatment and is thus available from the fertility center database.

    Measured: 2 years after pick up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Nov 2016 (estimated)
  2. Study startNov 2016
  3. Primary completionNov 2019 (estimated)
  4. Study completionNov 2020 (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 N/A
Primary purpose
Other
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02962466
Sponsor's protocol ID
BUN:143201628797
Acronym
MC_CC-Test
Status last verified
Oct 2018
First submitted
27 Oct 2016
Last updated
30 Oct 2018
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Publications

  • Van Vaerenbergh I, Adriaenssens T, Coucke W, Van Landuyt L, Verheyen G, De Brucker M, Camus M, Platteau P, De Vos M, Van Hecke E, Rosenthal A, Smitz J. Improved clinical outcomes after non-invasive oocyte selection and Day 3 eSET in ICSI patients. Reprod Biol Endocrinol. 2021 Feb 19;19(1):26. doi: 10.1186/s12958-021-00704-5.

    PubMed 33608027

Questions about this trial

What is this clinical trial studying?

A study testing CC-Test in people with Pregnancy, run by Universitair Ziekenhuis Brussel at 2 sites in Belgium.

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 5 inclusion and 5 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 30 Oct 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Belgium. 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.

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 Tom Adriaenssens, Msc. (+ 32 2 477 50 50, Tom.Adriaenssens@UZBrussel.be), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Clinical Pregnancy as observed by ultrasound (time frame: 2 months after embryo transfer). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02962466, which also lists 1 linked publication.

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 30 Oct 2018.

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Multicenter Prospective Cumulus Cell Test Study | AzTrials