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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04438616
Other study ID # 3042020
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date April 30, 2021

Study information

Verified date April 2020
Source Cairo University
Contact hussein H moalla, bachelor
Phone 02201021422480
Email husein_hatam@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

- Patients were randomly divided in to two groups by using computerized software ; the first group received flat magnetic attachment design while the second group received dome magnetic attachment design.which the inclusion criteria is completely edentulous patient ,Age range from 40 to 70 year old ,skeletal class 1, both sexes

- Implant stability will be measured for both groups using smart peg /osstell at the day of implant installation and after 2,4,8,12 weeks.

- Patient satisfaction measure in 2 weak and after 12 weak by Denture satisfaction questionnaire


Description:

- The selected patients will be informed of the nature of the research work and informed consent will be obtained then randomized in equal proportions between control group flat magnetic attachment design and study group dome magnetic attachment design technique

- Radiographic examination included a preoperative digital panoramic radiograph with 1:1 magnification for each patient as a primary survey to obtain an approximation of the available bone height and detect the presence of remaining roots and localized pathosis.

- All patients will receive complete denture before implant installation .Constructed as the following

- Primary impression to construct diagnostic cast and special tray .

- Secondary impression with selective pressure impression technique to have master caste and occlusion block

- Face bow transfer and centric relation record will be utilized to mount the master cast on semi adjuctable articulator ,then setting the teeth and trying the denture in patient mouth.

- Processing of acrylic and lab remounting ,then delivery of the denture.

- The complete denture will be duplication to be used as a guide to fabricate the radiographic stent after placement radio opaque marker in two lower canines then send patient to perform CBCT and these duplicate denture use as surgical template to place two implant.

- CBCT machine: planmeca / CBCT soft ware : blue sky / FOV: single arch mandible /voxel size :400 Mm ( KV:90 / MA: 8 / S:11,997)

- The CBCT examination where performed in radiology department / collage of dentistry /cairo university

- serial follow up CBCT not need

- Patients were randomly divided in to two groups by using computerized software ; the first group received flat magnetic attachment design while the second group received dome magnetic attachment design e. All surgeries were performed by the same prosthodontic.

- All surgical procedures were performed under strict aseptic conditions, all patients received infiltration local anesthesia (Articaine 4% 1:100 000 epinephrine).

- A crestal incision is made using No. 15 c blade extending over the crest of anterior mandible and a full mucoperiosteum flaps elevated to provide access to the alveolar ridge for implant installed.

- Full sequential drilling under copious saline irrigation will be made as indicated by the company guide lines. insertion of two implant in each group by the contra angle handpiece with special adaptor.(control and study groups)

- The flap will then be closed using interrupted 4/0 resorbable sutures.

- We connect magnetic attachment(flat,dome) for each groups on complete denture by pick up procedure at day of implant installation.

- Relief space from the denture for the magnetic attachment will be made and a rubber dam will be used to closed the under cute under the magnetic attachment. pickup material will be added in the relief area to connect the housing to the denture intra orally.

- Implant stability will be measured for both groups using smart peg /osstell at the day of implant installation and after 2,4,8,12 weeks.

- Patient satisfaction measure in 2 weak and after 12 weak by Denture satisfaction questionnaire


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 28
Est. completion date April 30, 2021
Est. primary completion date January 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria:

- completely edentulous patient.

- Age range from 40 to 70 year old

- Skeletal class 1

- Both sexes.

Exclusion Criteria:

- No intra oral soft and hard tissue pathology

- Heavy smokers more than 20 cigarettes per day.

- Patients with systemic disease that may affect normal healing.

- Patient with sever parafunctional occlusal activity.

- Immunodeficiency pathology, bruxism, stress situation (socially or professionally), emotional instability,.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
dome magnetic attachment
All patients will receive complete denture before implant installation . The CBCT examination should be take patients received infiltration local anesthesia A crestal incision is made using No. 15 c blade . Full sequential drilling under copious saline irrigation will be made . insertion of two implant by the contra angle handpiece with special adaptor We connect magnetic attachment(dome) on complete denture by pick up procedure at day of implant installation. Implant stability will be measured using smart peg /osstell at the day of implant installation and after 2,4,8,12 weeks. Patient satisfaction measure
flat magnetic attachment
All patients will receive complete denture before implant installation . The CBCT examination should be take patients received infiltration local anesthesia. A crestal incision is made using No. 15 c blade Full sequential drilling under copious saline irrigation will be made as indicated by the company guide lines. insertion of two implant by the contra angle handpiece with special adaptor We connect magnetic attachment(flat) on complete denture by pick up procedure at day of implant installation. Implant stability will be measured using smart peg /osstell at the day of implant installation and after 2,4,8,12 weeks. Patient satisfaction measure in 2 weak and after 12 weak by Denture satisfaction questionnaire

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

References & Publications (5)

Allen PF, McMillan AS, Walshaw D. A patient-based assessment of implant-stabilized and conventional complete dentures. J Prosthet Dent. 2001 Feb;85(2):141-7. — View Citation

Barão VA, Assunção WG, Tabata LF, Delben JA, Gomes EA, de Sousa EA, Rocha EP. Finite element analysis to compare complete denture and implant-retained overdentures with different attachment systems. J Craniofac Surg. 2009 Jul;20(4):1066-71. doi: 10.1097/SCS.0b013e3181abb395. — View Citation

Boerrigter EM, Geertman ME, Van Oort RP, Bouma J, Raghoebar GM, van Waas MA, van't Hof MA, Boering G, Kalk W. Patient satisfaction with implant-retained mandibular overdentures. A comparison with new complete dentures not retained by implants--a multicentre randomized clinical trial. Br J Oral Maxillofac Surg. 1995 Oct;33(5):282-8. — View Citation

Feine JS, Carlsson GE, Awad MA, Chehade A, Duncan WJ, Gizani S, Head T, Lund JP, MacEntee M, Mericske-Stern R, Mojon P, Morais J, Naert I, Payne AG, Penrod J, Stoker GT, Tawse-Smith A, Taylor TD, Thomason JM, Thomson WM, Wismeijer D. The McGill consensus statement on overdentures. Mandibular two-implant overdentures as first choice standard of care for edentulous patients. Montreal, Quebec, May 24-25, 2002. Int J Oral Maxillofac Implants. 2002 Jul-Aug;17(4):601-2. Review. — View Citation

Tallgren A. The continuing reduction of the residual alveolar ridges in complete denture wearers: a mixed-longitudinal study covering 25 years. J Prosthet Dent. 1972 Feb;27(2):120-32. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary name of measurement: Patient satisfaction Denture satisfaction questionnaire Patient satisfaction measure in 2 weak
Primary name of measurement: Patient satisfaction Denture satisfaction questionnaire Patient satisfaction measure in 12 weak
Secondary name of measurement: implant stability Measurement unit: ISQ \ Measurement device: Osstell device \ scale: 1-100 ISQ .measurement tool is smart peg attached to implant and hand-held probe. Implant stability will be measure at day of implant
Secondary name of measurement: implant stability Measurement unit: ISQ \ Measurement device: Osstell device \ scale: 1-100 ISQ .measurement tool is smart peg attached to implant and hand-held probe. Implant stability will be measure after 2 weak
Secondary name of measurement: implant stability Measurement unit: ISQ \ Measurement device: Osstell device \ scale: 1-100 ISQ measurement tool is smart peg attached to implant and hand-held probe. Implant stability will be measure after 4 weak
Secondary name of measurement: implant stability Measurement unit: ISQ \ Measurement device: Osstell device \ scale: 1-100 ISQ measurement tool is smart peg attached to implant and hand-held probe. Implant stability will be measure after 8 weak
Secondary name of measurement: implant stability Measurement unit: ISQ \ Measurement device: Osstell device \ scale: 1-100 ISQ measurement tool is smart peg attached to implant and hand-held probe. Implant stability will be measure after 12 weak
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