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A Prospective Multicenter Study to evaluate the feasibility and safety of pediatric tonsillectomy using BiZact tonsillectomy device

A Prospective Multicenter Study to evaluate the feasibility and safety of pediatric tonsillectomy using BiZact tonsillectomy device

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0010087
Enrollment
100
Registered
2024-12-27
Start date
2024-11-18
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

None listed

Interventions

None listed

Sponsors

Pusan National University Yangsan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: the ages from 3 to 18 years

Exclusion criteria

Exclusion criteria: Patients underwent unilateral tonsillectomy Patients underwent tonsillectomy using other energy device Patients underwent wide tonsillectomy due to malignancy

Design outcomes

Primary

MeasureTime frame
Postoperative pain(Wong-Baker FACES pain rating scale)

Secondary

MeasureTime frame
Postoperative hemorrhage(Classification of Postoperative Bleeding Episodes by Sarny S.9);Other postoperative complication;Operation time and intraoperative blood loss

Countries

Korea, Republic of

Contacts

Public ContactEui-Suk Sung

Pusan National University Yangsan Hospital

ch1oh@naver.com+82-55-360-2132

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026