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NCT03134001

Evaluation of Oral PCA Device - PCoA™ Acute

Completed NA Last updated 8 May 2017
What this trial tests

NA trial testing patients receiving oral analgesics via the PCoA™ Acute in Pain, Postoperative in 70 participants. Completed in 30 November 2015.

Timeline
1 June 2015
Primary endpoint
30 November 2015
30 November 2015

Quick facts

Lead sponsorDosentrx Ltd.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment70
Start date1 June 2015
Primary completion30 November 2015
Estimated completion30 November 2015

Drugs / interventions tested

Conditions studied

Sponsor

Dosentrx Ltd.

Who can join

Adults 18 to 80, any sex, with Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Randomized, open label, controlled pilot clinical study comprised hospitalized post operative patients receiving oral analgesics. The study aims to evaluate the safety, efficacy and usability of a novel pill dispensing system - PCoA™ Acute and compare it to the conventional procedure of nurse providing analgesics.

Publications & conference data

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

  1. Clinical Evaluation of a Novel Technology for Oral Patient-Controlled Analgesia, the <i>PCoA® Acute</i> Device, for Hospitalized Patients with Postoperative Pain, in Pilot Feasibility Study.
    Wirz S, Conrad S, Shtrichman R, Schimo K, et al · · 2017 · cited 5× · PMID 29093632 · DOI 10.1155/2017/7962135

Verify or expand the search:

Other recruiting trials for Pain, Postoperative

Currently open trials in the same condition.

Other Dosentrx Ltd. 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/NCT03134001.

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