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Lifetech AcuMark™ Sizing Balloon Post-Market Clinical Follow-up Study | Clinical Trials | Clareo Health

RECRUITINGNCT06700174

Lifetech AcuMark™ Sizing Balloon Post-Market Clinical Follow-up Study

The objective of this PMCF study is to: * confirm the safety and performance of the AcuMarkTM Sizing Balloon * identify previously unknown side-effects * monitor the identified side-effects (related ...

Lead sponsor: Lifetech Scientific (Shenzhen) Co., Ltd.•5 locations•View source on ClinicalTrials.gov

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Contacts

Shen Yuanyuan

CONTACT

86+18504356312 shenyuanyuan@lifetechmed.com

Fu Jiaxuan

CONTACT

86 13973207184 fujiaxuan@lifetechmed.com

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: November 21, 2024Terms

Trial snapshot

StatusRECRUITING

Phase—

Enrollment100

Start dateSep 2024

Last updatedNov 21, 2024

Condition

Atrial Septal Defect (ASD)

Locations shown

Ankara (Bilkent) City Hospital

Ankara

Gazi Yasargil Woman and Child Hospital

Diyarbakır

Gaziantep University Hospital

Gaziantep

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: November 21, 2024Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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