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NCT06158035

ED90 of Norepinephrine and Phenylephrine Boluses Under Intensive Treatment in Preeclamptic Patients

Status unknown NA Last updated 6 December 2023
What this trial tests

NA trial testing Norepinephrine in Adverse Effect in 80 participants. Status unknown.

Timeline
1 July 2025
Primary endpoint
30 December 2025
30 December 2025

Quick facts

Lead sponsorGeneral Hospital of Ningxia Medical University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment80
Start date1 July 2025
Primary completion30 December 2025
Estimated completion30 December 2025

Drugs / interventions tested

Conditions studied

Sponsor

General Hospital of Ningxia Medical University

Who can join

Adults 18 to 45, female only, with Adverse Effect. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to investigate the ED90 of norepinephrine and phenylephrine boluses for treating postspinal anesthesia hypotension under intensive treatment in preeclamptic patients during cesarean section

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Norepinephrine

Trials testing the same drug.

Other recruiting trials for Adverse Effect

Currently open trials in the same condition.

Other General Hospital of Ningxia Medical 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/NCT06158035.

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