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NCT04818190

DIEP (Deep Inferior Epigastric Artery Perforator) Flap Sensory Recovery Following Neurotization

Status unknown NA Last updated 4 October 2021
What this trial tests

NA trial testing Sensory neurotization in Sensitisation in 30 participants. Status unknown.

Timeline
1 September 2021
Primary endpoint
1 April 2023
1 May 2023

Quick facts

Lead sponsorUniversity of Manitoba
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingdouble
Primary purposetreatment
Enrollment30
Start date1 September 2021
Primary completion1 April 2023
Estimated completion1 May 2023
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

University of Manitoba

Who can join

18 and older, female only, with Sensitisation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to compare the sensory return of DIEP flaps with nerve connection to DIEP flaps with no nerve connection to see which is better. This research is being done because the presence of sensation in a reconstructed breast has been shown to improve patient-related quality of life following mastectomy reconstruction and is an important safety factor for prevention of burns and other flap injuries. Unfortunately, women who have breast skin excised during mastectomy are reconstructed with a traditional DIEP flap that does not restore sensation to the skin.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other University of Manitoba 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/NCT04818190.

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