Last reviewed · How we verify

NCT03391609

Peri-operative Dexmedetomidine Infusion in Pre-eclamptic Patients

Completed Phase 2, PHASE3 Last updated 26 February 2019
What this trial tests

Phase 2, PHASE3 trial testing placebo infusion in Pre-Eclampsia in 30 participants. Completed in 1 January 2019.

Timeline
18 June 2017
Primary endpoint
1 November 2018
1 January 2019

Quick facts

Lead sponsorAssiut University
PhasePhase 2, PHASE3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingtriple
Primary purposetreatment
Enrollment30
Start date18 June 2017
Primary completion1 November 2018
Estimated completion1 January 2019
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 19 to 40, female only, with Pre-Eclampsia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to investigate the effects of dexmedetomidine infusion on the stress response to intubation, postoperative analgesia, and renal functions (urinary output \[UOP\], creatinine and glomerular filtration rate \[GFR\]) in preeclamptic patient.

Publications & conference data

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

Verify or expand the search:

Other trials of Dexmedetomidine infusion

Trials testing the same drug.

Other recruiting trials for Pre-Eclampsia

Currently open trials in the same condition.

Other Assiut University 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/NCT03391609.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing