Crossover trial comparing the clinical results of complete dentures with the biofunctional prosthetic system and conventional procedures.

Crossover trial comparing the clinical results of complete dentures with the biofunctional prosthetic system and conventional procedures. - Comparison of the BPS and conventional procedures

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000016650

Enrollment

Registered

2015-02-27

Start date

2010-10-01

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

Edentulous

Interventions

Fabricating the new set of the complete dentures with BPS Fabricating the new set of the complete dentures with conventional procedure

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (a) healthy adult patient requiring a new set of complete dentures; (b) complete dentures worn for at least 3 years previously; and (c) patient is mentally receptive

Exclusion criteria

Exclusion criteria: (a) Participants with dysfunction disorders of the masticatory system, debilitating systemic disease or oral mucosal disease.

Design outcomes

Primary

Measure	Time frame
Oral Health-Related Quality of Life (OHR-QoL) Denture satisfaction Denture comparison questionnaire Number of adjustments	—

Countries

Japan

Contacts

Public ContactKen-ichi Matsuda

Osaka University Graduate School of Dentistry Department of Prosthodontics,Gerodontology and Oral Rehabilitation

digiflex@dent.osaka-u.ac.jp06-6879-2954

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026