Status:
COMPLETED
Effects of Two In-hospital Antepartum Interventions on Functional Ability and Quality of Life in Early Postpartum Women.
Lead Sponsor:
Western University, Canada
Conditions:
High-Risk Pregnancy
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The current standard of care for pregnant women deemed to be high-risk often involves recommending varying levels of activity-restriction, up to and including hospitalization. High levels of activity-...
Eligibility Criteria
Inclusion
- Hospitalized high-risk pregnant women in hospital for at least 7 days
- Diagnosed with gestational hypertension
- Diagnosed with preeclampsia (mild to moderate)
- Diagnosed with intrauterine growth restriction
- Single baby
- Expecting twins
- Expecting triplets
- Diagnosed with shortened cervix
- Diagnosed with threatened pre-term labour (not actively contracting)
Exclusion
- Diagnosed with symptomatic placenta previa (bleeding)
- Diagnosed with severe pre-eclampsia (immediate delivery)
- Diagnosed with conditions indicating a short term hospital stays of less than 7 days
- Diagnosed with infections
- Diagnosed with heart and renal disease
- Diagnosed with diabetes
- Diagnosed with metabolic bone disease
- Diagnosed with hyper-or-hypo-thyroidism
- Diagnosed with Cushing disease and anemia
- Women carrying more than 3 babies
Key Trial Info
Start Date :
October 30 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 30 2017
Estimated Enrollment :
9 Patients enrolled
Trial Details
Trial ID
NCT02239341
Start Date
October 30 2014
End Date
December 30 2017
Last Update
December 11 2023
Active Locations (1)
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1
London Health Sciences Centre
London, Ontario, Canada, N6A 5W9