Evaluation of quality of life and oral function in patients with drug-related osteonecrosis of the jaw

Evaluation of quality of life and oral function in patients with drug-related osteonecrosis of the jaw - Evaluation of quality of life and oral function in patients with drug-related osteonecrosis of the jaw

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000057902

Enrollment

100

Registered

2025-05-19

Start date

2024-03-26

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Medication related osteonecrosis of the jaw

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Age 20 or older at the time of consent Outpatient/Inpatient: No questions asked Gender: any or male or female Diagnosed with drug-related osteonecrosis of the jaw Patients who have received a thorough explanation of their participation in this study, and who have given their free and voluntary consent based on a thorough understanding of the subject's condition.

Exclusion criteria

Exclusion criteria: Patients with surgical recurrence Patients who refused to participate in this study Other patients deemed inappropriate as research subjects by the principal investigator

Design outcomes

Primary

Measure	Time frame
FACT H&N scores by treatment	—

Secondary

Measure	Time frame
Oral function tests by treatment	—

Countries

Japan

Contacts

Public ContactYuki Sakamoto

Kansai medical university medical center Oral surgery

s.yukioutdoor@gmail.com06699639420

Outcome results