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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	JPRN
Last refreshed on:	17 October 2023
Main ID:	JPRN-UMIN000016650
Date of registration:	27/02/2015
Prospective Registration:	No
Primary sponsor:	Osaka University Graduate School of Dentistry
Public title:	Crossover trial comparing the clinical results of complete dentures with the biofunctional prosthetic system and conventional procedures.
Scientific title:	Crossover trial comparing the clinical results of complete dentures with the biofunctional prosthetic system and conventional procedures. - Comparison of the BPS and conventional procedures
Date of first enrolment:	2010/10/01
Target sample size:	10
Recruitment status:	Complete: follow-up complete
URL:	https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000019326
Study type:	Interventional
Study design:	Cross-over Randomized
Phase:	Not selected

Countries of recruitment
Japan

Contacts

Name:	Ken-ichi Matsuda
Address:	1-8 Yamadaoka, Suita, Osaka, Japan Japan
Telephone:	06-6879-2954
Email:	digiflex@dent.osaka-u.ac.jp
Affiliation:	Osaka University Graduate School of Dentistry Department of Prosthodontics,Gerodontology and Oral Rehabilitation

Name:	Ken-ichi Matsuda
Address:	1-8 Yamadaoka, Suita, Osaka, Japan Japan
Telephone:	06-6879-2954
Email:	digiflex@dent.osaka-u.ac.jp
Affiliation:	Osaka University Graduate School of Dentistry Department of Prosthodontics,Gerodontology and Oral Rehabilitation

Key inclusion & exclusion criteria

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

Age minimum: 60years-old
Age maximum: 90years-old
Gender: Male and Female

Health Condition(s) or Problem(s) studied

Edentulous

Intervention(s)

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

Primary Outcome(s)

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

Secondary Outcome(s)

Secondary ID(s)

Source(s) of Monetary Support

none

Secondary Sponsor(s)

Ethics review

Status: YES
Approval date:
Contact:

Results

Results available:
Date Posted:
Date Completed:
URL:

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