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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03930862
Other study ID # Muscle activity
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 15, 2019
Est. completion date October 1, 2020

Study information

Verified date April 2019
Source Cairo University
Contact Lamees Hosame, Master
Phone 020-1020111367
Email Lamees_bota@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Will the use of locator attachment influence the muscle efficacy when compared to ball and socket attachment in mandibular implant overdenture? '


Description:

In this study we will use a two different types of attachments in implants overdenture in mandibular completely edentulous patients to increase the retention and stability of the denture and this can be recognized by record the masticatory function of the muscles of the mandibular jaw.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 12
Est. completion date October 1, 2020
Est. primary completion date October 1, 2020
Accepts healthy volunteers No
Gender All
Age group 45 Years to 65 Years
Eligibility Inclusion Criteria:

- Upper and lower completely edentulous patients. Acceptance of the existing denture if it is good, or constructing a new one if it is defected.

Patients with adequate bone quality and quantity. Tooth extracted not less than 6 month.

Exclusion Criteria:

1. Young patients.

2. Diseases affecting neuromuscular coordination.

3. TMJ diseases.

4. Soft tissue abnormalities.

5. Bony exostosis.

6. Parathyroid dysfunction

7. uncontrolled Diabetes

8. Radiotherapy to the neck or head

9. Pregnancy.

10. Drug and alcohol dependency.

11. Smokers.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Locator Attachment (positioner)
intra oral attachment

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Lamees Hosam Ramadan

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle Activity Digital Electromyogram 6 month
Secondary Patient Satisfaction: questionnaire questionnaire from zero to 10 where zero is completely unsatisfied and 10 is highly satisfied 6 month
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