Evaluation of clinical efficacy of medical device (light-guided needle for injection laryngoplasty) manufactured by Korean company: multicenter study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0006740

Enrollment

130

Registered

2021-11-11

Start date

2021-11-15

Completion date

Unknown

Last updated

2021-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : This study is a multicenter study led by "the Korean Society of Laryngology, Phoniatrics, and Logopedics" to collect expert opinions on vocal cord injection using a light guide drug

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Age 19-75, Those who do not lack decision-making ability/ Those who voluntarily sign the consent form for clinical participation

Exclusion criteria

Exclusion criteria: Patients who did not consent to this clinical trial / Patients with a history of previous treatment for vocal cord paralysis such as intra-vocal injection or laryngoplasty / Patients with a high risk of bleeding such as anticoagulants

Design outcomes

Primary

Measure	Time frame
The incidence of procedure-related complications during the procedure;Procedure time	—

Secondary

Measure	Time frame
Multidimensional voice analysis test	—

Countries

Korea, Republic of

Contacts

Public ContactMan Ki Chung

Samsung Medical Center

manki.chung@gmail.com+82-2-3410-1845

Outcome results