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Persisting complaints after hypertensive complications in pregnancy and the effects on daily functioning

Persisting complaints after hypertensive complications in pregnancy and the effects on daily functioning - Persisiting complaints after PE / HELLP and daily functioning.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31823
Enrollment
70
Registered
2008-02-20
Start date
2008-04-01
Completion date
Unknown
Last updated
2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pre-eclampsia toxic pregnancy

Interventions

None listed

Sponsors

Academisch Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Study group: para 1, after going trough a hypertensively complicated pregnancy; delivery has taken place maximally one year before the study; maximum duration of pregnancy: 32 weeks Control group: para 1, after going trough an uncomplicated pregnancy; delivery has taken place maximally one year before the study; minimal duration of pregnancy: 38 weeks.

Exclusion criteria

Exclusion criteria: Studygroup: mental, physical and social symptoms before the complicated pregnancy; current pregnancy. Control group: mental, physical and social symptoms before the complicated pregnancy; current pregnancy; postnatal hospitalization of mother and child or postnatal mortality.

Design outcomes

Primary

MeasureTime frame
Physical and mental symptoms or complaints and limitations in daily functioning are dependent study parameters. Events in or results from (complicated) pregnancy are in this study independent study parameters. The level of limitation is the main outcome of this study.

Secondary

MeasureTime frame
Personality characteristics and character are parameters that can effect the main outcome.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)