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NCT05136534: SPINOFAST

Spinal Versus Local Anesthesia for Hernia Repair

Completed NA Last updated 29 November 2021
What this trial tests

NA trial testing spinal anesthesia in Hernia, Inguinal in 132 participants. Completed in 12 February 2020.

Timeline
10 January 2019
Primary endpoint
12 February 2020
12 February 2020

Quick facts

Lead sponsorCampus Bio-Medico University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment132
Start date10 January 2019
Primary completion12 February 2020
Estimated completion12 February 2020
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Campus Bio-Medico University

Who can join

18 and older, any sex, with Hernia, Inguinal. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

patients underwent inguinal hernia repair; Group A patients received Subarachnoid anesthesia; Group B Patients underwent surgery with local anesthesia (Mepivacaine 2%) performed by the surgeon; Pain assessment was performed using a 0-10 Numerical Rating Scale (NRS). Intraoperative pain was assessed every 10 minutes,

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of spinal anesthesia

Trials testing the same drug.

Other recruiting trials for Hernia, Inguinal

Currently open trials in the same condition.

Other Campus Bio-Medico 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/NCT05136534.

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