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MLPA And Karyotyping, an Evaluation (M.A.K.E.).


- candidate number2373
- NTR NumberNTR845
- ISRCTNISRCTN47252164
- Date ISRCTN created22-jan-2007
- date ISRCTN requested12-jan-2007
- Date Registered NTR18-dec-2006
- Secondary IDs80-007029-98-07-047 
- Public TitleMLPA And Karyotyping, an Evaluation (M.A.K.E.).
- Scientific TitlePrenatal diagnosis: MLPA and/ or karyotyping in amniotic fluid; Diagnostic acurracy, patient outcome en costs.
- ACRONYMM.A.K.E.
- hypothesisThe present study will establish the suggested equivalent preclinical diagnostic accuracy of MLPA in a clinical setting.
- Healt Condition(s) or Problem(s) studiedFetal aneuploidy, Trisomy 13, Trisomy 18, Trisomy 21, Sex chromosome abnormalities
- Inclusion criteria1. Amniocentesis is performed; 2. The referral indication is advanced maternal age and/or increased risk after PNS; 3. Age > or = 18 years; 4. No language barriers; 5. Informed consent is given; 6. Singleton pregnancies.
- Exclusion criteriaOther referral indications: parent (s) with chromosome aberration, ultrasound abnormalities, previous child with chromosome aberration.
- mec approval receivedyes
- multicenter trialyes
- randomisedno
- group[default]
- Type-
- Studytypeintervention
- planned startdate 1-feb-2007
- planned closingdate1-jan-2009
- Target number of participants4500
- InterventionsBoth MLPA and Karyotyping are carried out. MLPA (multiplex ligation-dependent probe amplification) is a molecular genetic technique in prenatal diagnosis using amniotic fluid. In this study a commercially available kit, P095 is used (produced by MRC Holland and widely tested). The MLPA-result is known in 2-4 days. To perform MLPA 2-4ml of amniotic fluid is required. Such an amount is available since routinely 15-20 ml of amniotic fluid is obtained. If there is too little amniotic fluid (<12ml), MLPA will not be carried out in the study. Karyotyping is carried out without any changes. The result is known in 2-3 weeks.
- Primary outcomeDiagnostic accuracy, technical performance (inconclusive or missing results), technical capacity.
- Secondary outcomePatient anxiety and distress, cost-effectiveness, unexpected findings and patient preference.
- Timepoints
- Trial web sitehttp://www.makestudy.nl
- statusplanned
- CONTACT FOR PUBLIC QUERIES Elisabeth Boormans
- CONTACT for SCIENTIFIC QUERIESProf. Dr. J.M.M. Lith, van
- Sponsor/Initiator Onze Lieve Vrouwe Gasthuis (OLVG), Department of Obstetrics and Gynaecology, Academic Medical Center (AMC), Department of Obstetrics and Gynaecology
- Funding
(Source(s) of Monetary or Material Support)
ZON-MW, The Netherlands Organization for Health Research and Development
- PublicationsN/A
- Brief summaryFor the past 30 years karyotyping is the gold standard in prenatal diagnosis for the detection of chromosomal aberrations in the fetus, in particular trisomy 21 (Down syndrome). The main indications for traditional karyotyping (TKT) in the Netherlands are advanced maternal age and increased risk based on prenatal screening tests (PNS) . The annual numbers of maternal age-based invasive procedures for TKT are decreasing1, in contrast to the numbers of PNS. This is due to a shift of the maternal age distribution, with a relative increase of elderly pregnant women making use of PNS, an increased demand of pregnant women, augmented by a change in government policy allowing PNS (combined test, triple test) for risk estimation of Down syndrome (DS). MLPA (multiplex ligation-dependent probe amplification) is a new molecular genetic technique in prenatal diagnosis using amniotic fluid. It is a potential alternative test for detecting aneuploidies. Compared to TKT, MLPA has four potential advantages: (1) The result is known in 2-4 days instead of 3 weeks (2) The procedure is considerably less labour intensive (3) The test requires less amniotic fluid (2-4 ml instead of 20 ml) (4) MLPA is suitable for high throughput testing. Previous preclinical evidence suggests equivalence of MLPA and TKT regarding test performance (accuracy in detection of common occurring chromosome aberrations).
- Main changes (audit trail)
- RECORD18-dec-2006 - 23-jan-2007


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