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NCT03941327

Do AxoGuard Implants Decrease Shoulder Disability After Neck Dissections

Status unknown NA Last updated 7 May 2019
What this trial tests

NA trial testing AxoGuard Nerve Cuff in Spinal Accessory Nerve Injury in 100 participants. Status unknown.

Timeline
1 May 2019
Primary endpoint
1 May 2020
1 May 2020

Quick facts

Lead sponsorUniversity of Mississippi Medical Center
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment100
Start date1 May 2019
Primary completion1 May 2020
Estimated completion1 May 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Mississippi Medical Center

Who can join

18 and older, any sex, with Spinal Accessory Nerve Injury or Cervical Lymphadenopathy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine whether Axoguard nerve protectors have a role in preventing shoulder disability and pain following spinal accessory nerve sparing neck dissections.

Publications & conference data

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

  1. Modern Trends for Peripheral Nerve Repair and Regeneration: Beyond the Hollow Nerve Guidance Conduit.
    Carvalho CR, Oliveira JM, Reis RL. · · 2019 · cited 201× · PMID 31824934 · DOI 10.3389/fbioe.2019.00337

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Other University of Mississippi Medical Center trials

Trials by the same sponsor.

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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/NCT03941327.

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