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NCT01380912

Can Injection of Methylprednisoloneacetate 80 mg, in the Cavity After Mastectomy for Primary Breast Cancer, at the Time of Removal of the Drain, Prevent Seroma Formation?

Status unknown Last updated 23 June 2011
What this trial tests

trial testing methylprednisoloneacetate in Breast Cancer in 160 participants. Status unknown.

Timeline
1 August 2010
Primary endpoint
1 August 2011
1 August 2012

Quick facts

Lead sponsorCopenhagen University Hospital at Herlev
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment160
Start date1 August 2010
Primary completion1 August 2011
Estimated completion1 August 2012
Sites2 locations across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Copenhagen University Hospital at Herlev

Who can join

Adults 18 to 90, female only, with Breast Cancer. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

A randomised double-blinded study, in which the patients either get methylprednisoloneacetate or saline solution in the mastectomy cavity to evaluate the efficacy of methylprednisoloneacetate in preventing seroma in patients operated for primary breast cancer.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Breast Cancer

Currently open trials in the same condition.

Other Copenhagen University Hospital at Herlev 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/NCT01380912.

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