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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03804177
Other study ID # perio25111987
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date February 10, 2019
Est. completion date April 30, 2022

Study information

Verified date January 2019
Source Cairo University
Contact ahmed Nasser, Msc
Phone 00201094959526
Email ahmedelsawi8787@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The concept of immediate implant placement at the time of tooth extraction was first introduced by Schulte et al. on animal studies. Since then, many follow‑up studies examining different variables have supported the concept of immediate implant placement. pioneered a major contribution to immediate implant placement in human studies which recommended the insertion of an implant into a fresh extraction socket.

They advocated immediate implant placement primarily to reduce the number of surgical interventions needed to perform an implant‑supported rehabilitation and shorten the treatment time.

Placement of implants immediately into extraction sites allow the surgeon to idealize the position of the implant appropriately with a better rehabilitation of the normal contour to the facial aspect of the final restoration.

Immediate implant placement in fresh extraction sockets was reported to reduce alveolar bone resorption. Better esthetic outcomes were achieved including the prosthetic crown length in harmony with the adjacent teeth, natural scalloping and easier distinct papillae to achieve and maximum soft tissue support.

Hyaluronic acid is a glycosaminoglycan, this unique molecule is implicated In a variety of biological functions including structural integrity, and the regulation of embryologic development. It is described as a natural organic substance, with physiological therapy activity, main component of the extracellular matrix of many tissues such as the skin, synovial joints and periodontal tissues .


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 24
Est. completion date April 30, 2022
Est. primary completion date February 10, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Age: 18-60.

2. Systemically healthy patients indicated for single or multiple immediate implants in anterior and premolar region.

3. Absence of any peri-apical pathosis.

4. Patients with intact buccal plate of bone.

5. Patients with adequate bone volume for the dental implant procedure.

6. Patient consent approval and signing.

Exclusion Criteria:

- 1. Smokers. 2. Systemic disease that may affect the final outcome of the surgical procedure.

3. No or poor patient's compliance. 4. Patients with psychological problems. 5. Pathology at the site of intervention. 6. Pregnant patients. 7. Patients refuse to sign an informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
immediate implant placement with melatonin hyaluronic acid vit C
immediate implant placement with melatonin and hyaluronic acid and systemic administration vitamin C
immediate implant placement without melatonin hyaluronic acid vit C
immediate implant placement without melatonin and hyaluronic acid and systemic administration vitamin C

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

References & Publications (2)

El-Gammal MY, Salem AS, Anees MM, Tawfik MA. Clinical and Radiographic Evaluation of Immediate Loaded Dental Implants With Local Application of Melatonin: A Preliminary Randomized Controlled Clinical Trial. J Oral Implantol. 2016 Apr;42(2):119-25. doi: 10.1563/aaid-joi-D-14-00277. Epub 2015 Jun 23. — View Citation

Lee JH, Kim J, Baek HR, Lee KM, Seo JH, Lee HK, Lee AY, Zheng GB, Chang BS, Lee CK. Fabrication of an rhBMP-2 loaded porous ß-TCP microsphere-hyaluronic acid-based powder gel composite and evaluation of implant osseointegration. J Mater Sci Mater Med. 2014 Sep;25(9):2141-51. doi: 10.1007/s10856-014-5250-0. Epub 2014 Jun 14. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary implant stability implant stability by ostell 6 months
Secondary soft tissue healing soft tissue healing by likert scale (0 indicate complete soft tissue Closure (no line of fibrin) , 1 indicate complete closure (thin line of fibrin) , 2 indcate complete closure (fibrin) , 3 indicate in complete closure (dehiscence ) , 4 indicate incomplete closure (necrosis) 6 months
See also
  Status Clinical Trial Phase
Completed NCT03691467 - the Effect of Topical Application of Hyaluronic Acid on Immediate Dental Implant Phase 4
Completed NCT03689998 - Evaluation of Melatonin Application of Immediate Dental Implant Phase 4
Not yet recruiting NCT04449302 - Evaluation of Papilla Index Around Immediate Mandibular Molar Implants Using Customized Healing Abutment Versus Submerged Healing N/A
Not yet recruiting NCT03692026 - Assessment of Immediate Implant Stability When Adding Mixture of Hyaluronic Acid and Melatonin Phase 4
Completed NCT02864862 - Esthetic Outcomes Following Immediate Implant Combine With Soft Tissue Augmentation Phase 4
Completed NCT04343833 - Immediate Implants in the Aesthetic Zone N/A
Active, not recruiting NCT03183349 - Immediate Implant Placement With Platlet Rich Fibrin as Space Filling Material Versus the Use of Deprotienized Bovine Bone (Tutogen) in Maxillary Premolars. N/A
Completed NCT05101941 - Immediate Dental Implant Placed in the Presence of Chronic Inflammatory Periapical Lesions N/A