This is a retrospective study to make use of existing MRIs made from pregnant women who suspected a complication after bariatric surgery in pregnancy to make 3D replicas.
ID
Bron
Verkorte titel
Aandoening
N/A
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Producing 3D replicas of the pelvis, the uterus including placenta, amniotic fluid and child, the pelvic floor and the birth canal of the pregnant woman by using already made and existing MRIs.
Achtergrond van het onderzoek
To improve the outcomes for extreme preterm infants, the Perinatal Life Support (PLS) consortium is developing a medical device - an artificial womb (AW) - that supports the growth of this extremely premature group better and safer outside the uterus. Rather than exposing the preterm child to the stressful treatments of the NICU, the AW retains the liquid environment of the natural uterus. In order to ensure that the transfer of the premature child runs as smoothly as possible, a device with artificial amniotic fluid is developed to accommodate the premature child during a vaginal birth. The child will be placed in the AW from this “collection bag”. In order to develop a device that optimally matches the birth canal of the mother during delivery, we want to produce realistic replicas of the uterus, placenta, fetus in the uterus, pelvic floor and birth canal. In this retrospective study we will be using existing MRI images of pregnant women, in order to model these anatomical parts in 3D software.
Doel van het onderzoek
This is a retrospective study to make use of existing MRIs made from pregnant women who suspected a complication after bariatric surgery in pregnancy to make 3D replicas.
Onderzoeksopzet
The patients will be contacted by the coordinating investigator and in case of consent these patients will be sent a PIF.
Onderzoeksproduct en/of interventie
No interventions, study is retrospective.
Algemeen / deelnemers
Wetenschappers
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- MRI is made at an amenorrhea period of 20-30 weeks.
- Pregnant patients suspected of having a complication after bariatric surgery and who have had an MRI.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Major anatomical abnormalities of the fetus and birth canal.
- Placenta previa.
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Toelichting
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL8681 |
| Ander register | METC MMC : TBD |