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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: IRCT
Last refreshed on: 22 February 2018
Main ID:  IRCT2014070118202N2
Date of registration: 2014-07-10
Prospective Registration: Yes
Primary sponsor: Invicta s.z o.o.
Public title: Routine use of next generation sequencing (NGS) for preimplantation genetic diagnostics (PGD) of blastomeres obtained from embryos on day 3 in fresh IVF cycles.
Scientific title: Routine use of next generation sequencing (NGS) for preimplantation genetic diagnostics (PGD) of blastomeres obtained from embryos on day 3 in fresh IVF cycles.
Date of first enrolment: 2014-08-01
Target sample size: 28
Recruitment status: Complete
URL:  http://en.irct.ir/trial/16581
Study type:  interventional
Study design:  Randomization: Not randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Diagnostic.  
Phase:  N/A
Countries of recruitment
Poland
Contacts
Name: Judyta Zabielska   
Address:  ul. Trzy lipy 3 Gdansk Poland
Telephone: 00485858 58 810
Email: judyta.zabielska@invicta.pl
Affiliation:  Invicta Gdansk
Name: Judyta Zabielska   
Address:  GPNT ul. Trzy lipy 3 Gdansk Poland
Telephone: 00485858 58 810
Email: judyta.zabielska@invicta.pl
Affiliation:  Invicta Fertility and Reproductive Centre
Key inclusion & exclusion criteria
Inclusion criteria: Incusion:
1. Patients undergoing in vitro fertilization in Invicta Fertility and Reproductive Centre s. z o.o. in time frame from 08.2014 to 01.2015

Exclusion:
1. Patients who did not received embryo transfer in first cycle
2. Lack of data/results according to 5 verifications (that means 6-8 week after embryo transfer)

Exclusion criteria:

Age minimum: 31 years
Age maximum: 38 years
Gender: Both
Health Condition(s) or Problem(s) studied
Female infertility, unspecified
infertility.
Female infertility, unspecified
Intervention(s)
Next Generation Sequencing Preimplantation Genetic Diagnosis embryo selection
Diagnosis
Next Generation Sequencing Preimplantation Genetic Diagnosis embryo selection.
Primary Outcome(s)
Pregnancy rate. Timepoint: on 6 weeks and 1-3 days. Method of measurement: clinical poregnancy (as ultrasound fetal heartbeat detection).
Secondary Outcome(s)
Implantation rate. Timepoint: 7 day after tansfer. Method of measurement: blood serum beta-HCG concentration.
Secondary ID(s)
Source(s) of Monetary Support
Invicta s.z o.o.
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Komisja Bioetyczna przy Okregowej Izbie Lekarskiej
Results
Results available:
Date Posted:
Date Completed:
URL:
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