Last reviewed · How we verify

NCT03810547

Abdominoplasty Under Spinal Anesthesia

Completed NA Last updated 22 January 2019
What this trial tests

NA trial testing Propofol 10 Mg/mL Intravenous Emulsion in Spinal Anesthesia Suitability for Abdominoplasty in 200 participants. Completed in 31 December 2018.

Timeline
30 January 2017
Primary endpoint
30 April 2018
31 December 2018

Quick facts

Lead sponsorAin Shams University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposesupportive care
Enrollment200
Start date30 January 2017
Primary completion30 April 2018
Estimated completion31 December 2018
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Ain Shams University

Who can join

Adults 18 to 55, any sex, with Spinal Anesthesia Suitability for Abdominoplasty. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

100 patients undergoing abdominoplasty under spinal anesthesia. 100 patients undergoing abdominoplasty under general anesthesia

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Abdominoplasty under Spinal Anesthesia: A Feasibility Study.
    Metry AA, Nakhla GM, Wahba WZ, Wahba RM, et al · · 2019 · cited 3× · PMID 31198238 · DOI 10.4103/aer.aer_69_19

Verify or expand the search:

Other Ain Shams 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/NCT03810547.

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