Intravenous Labetalol Versus Hydralazine in Preeclampsia
NCT ID: NCT06360601
Last Updated: 2024-12-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE1/PHASE2
40 participants
INTERVENTIONAL
2024-04-01
2024-12-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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Labetalol group
Labetalol Injection
Labetalol intravenous infusion 20ml/hr
Hydralazine group
HydrALAZINE Injection
Hydralazine intravenous infusion 5mg/hr
Interventions
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Labetalol Injection
Labetalol intravenous infusion 20ml/hr
HydrALAZINE Injection
Hydralazine intravenous infusion 5mg/hr
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
\-
25 Years
45 Years
FEMALE
No
Sponsors
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Tanta University
OTHER
Responsible Party
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Mai Kamal
Lecturer of anaesthesia
Locations
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Tanta Univeristy hospitals
Tanta, , Egypt
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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36264PR589/3/24
Identifier Type: -
Identifier Source: org_study_id