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NCT04186091

Perfusion Index Predicts Post-spinal Hypotension in Obese Parturients for Cesarean Section

Completed Last updated 4 December 2019
What this trial tests

trial testing correlation between baseline perfusion index and decrease in systolic blood pressure post spinal induction in Perfusion Index Predicts Post-spinal Hypotension in 50 participants. Completed in 30 July 2018.

Timeline
1 April 2017
Primary endpoint
9 July 2018
30 July 2018

Quick facts

Lead sponsorCairo University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment50
Start date1 April 2017
Primary completion9 July 2018
Estimated completion30 July 2018
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 18 to 40, female only, with Perfusion Index Predicts Post-spinal Hypotension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hypotension is a common adverse effect of spinal anesthesia during caesarean section especially in obese patients. The aim of this study is to find out the correlation between baseline PI and post spinal hypotension in obese parturient.

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 Cairo University trials

Trials by the same sponsor.

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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/NCT04186091.

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