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NCT05586373: DIPROFEN

Ibuprofen vs Dipyrone After C-section in Preeclampsia

Completed Phase 4 Last updated 9 June 2023
What this trial tests

Phase 4 trial testing medication 1 in Preeclampsia in 74 participants. Completed in 31 May 2023.

Timeline
15 October 2022
Primary endpoint
31 May 2023
31 May 2023

Quick facts

Lead sponsorInstituto Materno Infantil Prof. Fernando Figueira
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment74
Start date15 October 2022
Primary completion31 May 2023
Estimated completion31 May 2023
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Instituto Materno Infantil Prof. Fernando Figueira

Who can join

14 and older, female only, with Preeclampsia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this randomized, triple-masked clinical trial is to compare the effectiveness and safety of the use of ibuprofen versus dipyrone for postoperative analgesia in postpartum women with preeclampsia undergoing cesarean section. The main question it aims to answer are: * Postoperative pain is similar; * The frequency of acute kidney injury is similar. Researchers will compare one group that will receive dipyrone and the other group that will receive ibuprofen to see if Postoperative pain are different between groups or development of acute kidney injury each group is different.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Preeclampsia

Currently open trials in the same condition.

Other Instituto Materno Infantil Prof. Fernando Figueira trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05586373.

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