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Efficacy of oral Furosemide in Postpartum Hypertension in Patients with Severe Preeclampsia in Kousar Hospital

Efficacy of oral Furosemide in Postpartum Hypertension in Patients with Severe Preeclampsia in Kousar Hospital

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014031717041N1
Enrollment
90
Registered
2014-04-15
Start date
2013-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

severe preeclampsia. Severe pre-eclampsia

Interventions

Intervention 1: After spontaneous onset of postpartum diuresis and discontinuation of intravenous magnesium sulfate , patients were randomly assigned to receive 20 mg oral furosemide daily for 5 day
Prevention
After spontaneous onset of postpartum diuresis and discontinuation of intravenous magnesium sulfate , patients were randomly assigned to receive 20 mg oral furosemide daily for 5 days with20 meq ora
After spontaneous onset of postpartum diuresis and discontinuation of intravenous magnesium sulfate , patients in control group receive no therapy.

Sponsors

Vice-Chancellor for research of Qazvin University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients delivered of a pregnancy at or greater than 20 weeks of gestation and diagnosed with severe preeclampsia. exclusion criteria: patients who had hypokalemia ( serum potassium less than 3 meq/l) on admission; patients who were already taking diuretics or potassium supplements for any reason; patients who demonstrated any hemodynamic instability surrounding the events of delivery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Assessment of mean of systolic and diastolic blood pressure in patients with severe preeclampsia. Timepoint: third day after delivery every 4 hours. Method of measurement: manometer.

Secondary

MeasureTime frame
Amount of weight loss after delivery. Timepoint: first and third day after delivery. Method of measurement: mechanical personal scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMona Shariati

Qazvin University of Medical Science

mshariati@qums.ac.ir+98 28 1223 6374

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026