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Study identifier: NCT07025304 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Post-Market Clinical Study to Evaluate the Safety and Effectiveness of REFLEX ULTRA 45 for Coblation Inferior Turbinate Reduction in China

Condition: Nasal Obstruction Due to Inferior Turbinate Hypertrophy  ·  Sponsor: Smith & Nephew, Inc.

PhaseNA
Planned participants105
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

The study is a prospective, multi-center, post-market clinical study to evaluate the safety and effectiveness of REFLEX ULTRA 45 for the coblation inferior turbinate reduction in China. The study product is REFLEX ULTRA 45 (EIC4845-01/EICA4845-01). Also it needs to be performed with the controller system COBLATOR II or WEREWOLF. The sample size is 105 subjects with approximate 6 sites in China mainland.

This description comes directly from the study's public registry record.

Talk to the study team

Cathy Xiao  ·  +86 18221637315  ·  Cathy.xiao@smith-nephew.com

Julian Yang  ·  +86 18101802151  ·  Julian.yang@smith-nephew.com

Always discuss trial participation with your own doctor first.

Locations (6)

The First Affiliated Hospital, Sun Yat-sen UniversityGuangzhou, Guangdong, ChinaRecruiting
The Third Affiliated Hospital, Sun Yat-sen UniversityGuangzhou, Guangdong, ChinaRecruiting
Henan Provincial People's HospitalZhengzhou, Henan, ChinaRecruiting
Jiangsu Province HospitalNanjing, Jiangsu, ChinaRecruiting
China-Japan Union Hospital of Jilin UniversityChangchun, Jilin, ChinaRecruiting
Sir Run Run Shaw Hospital Affiliated with Zhejiang University School of MedicineHangzhou, Zhejiang, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07025304