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Good quality soft tissue determines the possibility not only to obtain full primary wound closure during the bone defect reconstruction, but also assures effective implant treatment and stability of peri-implant condition.Moreover, it is very important to assure the proper emergence profile of the implant supported restorations, which give the opportunity to achieve the highest aesthetic appearance. In the long-term, the correct width and thickness of the attached keratinized tissue is the key point to ensure the stable position of the mucosal line around the implant's neck. The promising outcomes of laser on soft and hard tissue have been demonstrating in a variety of studies. Therefore, the aim of this clinical study is to evaluate the efficacy of LLDLT on enhancing osseointegration and on the peri-implant mucosal tissue around delayed dental implants.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| With laser | Experimental |
| |
| Without laser | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Dental implant + LLDL | Other | implant placement in the posterior areas and implants will be placed with application of LLDL. Preparation of the alveolus for delayed dental implant placement will be done and LLDL application according to manufacturer instructions |
| Measure | Description | Time Frame |
|---|---|---|
| Change in marginal bone loss | To assess the change in marginal bone loss, the linear distance from a fixed reference point-typically the implant shoulder or CEJ-to the highest level of bone-to-tooth/implant contact is measured. | 2 weeks, 1month, 2 months, and 6 months |
| Change in in implant stability | Ostell device will be used to assess implant stability | Immediately after surgery, 2 months and 6months postoperative. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in bone density | Radiographic examination of the patients will be done firstly pre-operative then at six months follow-up period post-operative by using CBCT device | 2 weeks, 1month, 2 months, and 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Kafr El-sheikh University | Kafr Elsheikh | Egypt |
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| ID | Term |
|---|---|
| D015921 | Dental Implants |
| ID | Term |
|---|---|
| D003764 | Dental Materials |
| D001697 | Biomedical and Dental Materials |
| D017266 | Dental Prosthesis |
| D011476 | Prosthodontics |
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| Dental implant | Other | It includes ten patients seeking for implant placement at the posterior areas and those patients will be received their implants only without application of LLDL . |
|
| D003813 |
| Dentistry |
| D019736 | Prostheses and Implants |
| D004864 | Equipment and Supplies |
| D008420 | Manufactured Materials |
| D013676 | Technology, Industry, and Agriculture |