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NCT06762860

Intravenous Granisetron Vs Dexmedetomidine on Postspinal in the Cesarean Section.

Status unknown NA Last updated 9 January 2025
What this trial tests

NA trial testing Dexmedetomidine in Postspinal Shivering in 99 participants. Status unknown.

Timeline
1 January 2024
Primary endpoint
30 January 2025
28 February 2025

Quick facts

Lead sponsorMinia University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment99
Start date1 January 2024
Primary completion30 January 2025
Estimated completion28 February 2025
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Minia University

Who can join

Adults 20 to 45, female only, with Postspinal Shivering. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The Aim of this study is to investigate and compare the efficacy of intravenous Dexmedetomidine (0.3 ug/kg) versus intravenous Granisetron (3 mg) in the prevention of shivering in parturient undergoing cesarean section under spinal anesthesia.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Dexmedetomidine

Trials testing the same drug.

Other Minia 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/NCT06762860.

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