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NCT06592027: Precedex

Dexmedetomidine for Attenuation of Pressor Response

Completed Phase 4 Last updated 19 September 2024
What this trial tests

Phase 4 trial testing PRECEDEX INJ★ 2ML in Pressor Response in 60 participants. Completed in 30 May 2024.

Timeline
1 February 2024
Primary endpoint
1 May 2024
30 May 2024

Quick facts

Lead sponsorTheodor Bilharz Research Institute
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment60
Start date1 February 2024
Primary completion1 May 2024
Estimated completion30 May 2024
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Theodor Bilharz Research Institute

Who can join

Adults 18 to 60, any sex, with Pressor Response. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Direct laryngoscopy and tracheal intubation are usually associated by hemodynamic changes due to increased sympathoadrenal activity which could precipitate serious negative effects in compromised patients . The pressor response could be blunted by dexmedetomidine which is a selective alpha 2 agonist which might provide hemodynamic stability during tracheal intubation.

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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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/NCT06592027.

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