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OpenTrials
Completed

NCT Number: NCT06650280

Assessment of Rapid Osseointegration of Dental Implants with Different Coatings

The study will assess early osseointegration of dental implant with three different coating materials through secondary implant stability

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Key information

Conditions

Dental Implants Hyaluronic Acid

Age range

18 year–49 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Dentistry, MSA University

Giza, Egypt

About this study

Dental implants with sandblasted acid itched coating, nano-hydroxyapatite coating, and hyalouronic acid coating will be placed in the posterior maxilla to restore a missing tooth. Implant stability by the use of Ostell will be measured immediately post-operative, 4, 6, and 12 weeks post-operative.

marginal bone loss around the implants will be compared immediately after final restoration delivery and after one year

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with missing at least one maxillary posterior tooth
  • Patients free from any systemic disease
  • Patients who approve to be included in the trial and sign the informed consent
  • Patients with no intra-bony defect.
  • Adults aged 18 years old and above

Exclusion criteria

  • Patients who are allergic to titanium
  • Heavy smoker patient
  • Patients receiving chemotherapy or radiotherapy
  • Patients who refused to be included in the trial

Treatment and study plan

Hyaluronic Acid (HA)

Other

hyaluronic acid coated implants will be placed in posterior maxilla to evaluate rapid osseointegration

nano-hydroxyapatite

Other

nano-hydroxyapatite coated implants will be placed in posterior maxilla to assess rapid osseointegration

sandblasted acid etched

Other

SLA coated implants will be placed in posterior maxilla and implant stability will be evaluated

Primary outcomes

  1. rapid osseintegration

    Time frame: immediately post-operative, 4, 6, and 12 weeks post-operative

    rapid osteointegration of dental implants will be evaluated by the use of Ostell device which measures primary and secondary stability expressed as ISQ measures ranging from zero till 90

Secondary outcomes

  1. marginal bone loss

    Time frame: immediately after final restoration delivery and one year post-operative

    the bone height from implant's platform till implant's tip will be measured and compared between immediately after final restoration delivery and after one year

Sponsors and collaborators

Lead sponsor

October University for Modern Sciences and Arts

Other

Registry information

Official study title

Assessment of Osseointegration of Dental Implants with Three Different Coatings for Early Loading Purpose and Marginal Bone Loss in the Posterior Maxilla. a Randomized Clinical Trial

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Oct 21, 2024
Registry last updated
Oct 21, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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