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

Completed

• Conditions: Pre-eclampsia; toxic pregnancy; 10026908

• Registration Number: NL-OMON31823
• Lead Sponsor: Academisch Ziekenhuis Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 70

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

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.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Physical and mental symptoms or complaints and limitations in daily functioning<br /><br>are dependent study parameters. Events in or results from (complicated)<br /><br>pregnancy are in this study independent study parameters. The level of<br /><br>limitation is the main outcome of this study.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Personality characteristics and character are parameters that can effect the<br /><br>main outcome.</p><br>