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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02951507
Other study ID # CEBD-CU-2016-10-232
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 29, 2016
Last updated October 31, 2016
Start date January 2017

Study information

Verified date October 2016
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority Egypt: Ministry of Higher Education
Study type Interventional

Clinical Trial Summary

Comparison of new design of extra coronal castable precision attachment (OT unilateral attachment) and conventional partial denture in patient satisfaction and biting force.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 42
Est. completion date
Est. primary completion date December 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria:

- patients with unilateral mandibular distal extension area

- Normal crown/root ratio of last premolar

- co-operative patients

Exclusion Criteria:

- completely edentulous patient

- few remaining teeth

- patients exposed to radiotherapy and chemotherapy

- patients with maxillary or mandibular defect

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms

  • Patient Acceptance of Health Care

Intervention

Other:
O T unilateral attachment
O T unilateral attachment system
New design of extracoronal attachment system
O T unilateral attachment

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary Patient satisfaction OHIP-14 questionnaire 12 months Yes
Secondary Biting force 12 months Yes
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