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Keep this study
Lead
Oxford University Hospitals NHS Trust
With
University of Cambridge
Prospective feasibility study with two arms; (i) case-control comparisons of saccadic reaction time distributions between patients with preterm pre-eclampsia, age- and gestation-matched pregnant controls and age-matched female non-pregnant controls \[cross-sectional analysis\]; (ii) intra-individual comparisons of antenatal and postnatal saccadic reaction time distributions of patients with preterm pre-eclampsia \[longitudinal analysis\].
Age
18–any
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
1. Age ≥ 18 years
2. Confirmed diagnosis of pre-eclampsia, as defined by the International Society for the Study of Hypertension in Pregnancy (ISSHP)
3. Gestational age \< 35+0 weeks
4. Participant is willing and able to give informed consent
1. Age ≥ 18 years
2. Absence of essential hypertension and pre-eclampsia or pregnancy-induced hypertension in current and previous pregnancies
3. Gestational age \< 35+0 weeks
4. Participant is willing and able to give informed consent
2. Use of medication (other than vitamin supplements \[cases and controls\] and those for treatment or prevention of pre-eclampsia \[cases\]) during pregnancy
Clareo Health | Saccadic Reaction Time and Preterm Pre-eclampsia
