Last reviewed · How we verify

NCT03527784

Prestoma-Trial for Parastomal Hernia Prevention

Terminated NA Last updated 5 November 2018
What this trial tests

NA trial testing Parietene Macro in Rectal Adenocarcinoma in 14 participants. Terminated before completion.

Timeline
3 May 2018
Primary endpoint
29 October 2018
29 October 2018

Quick facts

Lead sponsorUniversity of Oulu
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment14
Start date3 May 2018
Primary completion29 October 2018
Estimated completion29 October 2018
Sites6 locations across Finland

Drugs / interventions tested

Conditions studied

Sponsor

University of Oulu

Who can join

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

Sponsor's own description

Prestoma Trial is designed to compare the safety and efficiency of three different meshes and techniques to prevent parastomal hernia after laparoscopic or robotic-assisted abdominoperineal resection for rectal adenocarcinoma.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Rectal Adenocarcinoma

Currently open trials in the same condition.

Other University of Oulu 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/NCT03527784.

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