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Assessment of Osseointegration Properties of Nano-Hydroxy Apatite Coated Titanium Implant

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October University for Modern Sciences and Arts

Status

Completed

Conditions

Implant Site Reaction

Treatments

Other: nano-hydroxy apatite coated titanium implants
Other: sandblasted large acid itched coated titanium implant

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

the purpose of this trial is to evaluate the osseointegration properties of nano-hydroxy apatite coated titanium implants in posterior maxilla. 30 patients will be included in this trial divided into two groups, control and intervention. Primary and secondary implant stability will be measured

Enrollment

30 patients

Sex

All

Ages

18 to 49 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  1. Patients who are allergic to titanium
  2. Heavy smoker patient
  3. Patients receiving chemotherapy or radiotherapy
  4. Patients who refused to be included in the trial

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 2 patient groups

Nano-hydroxy apatite arm
Experimental group
Description:
in this groups patients will receive nano-hydroxy apatite coated titanium implants
Treatment:
Other: nano-hydroxy apatite coated titanium implants
SLA arm
Active Comparator group
Description:
in this group patients will receive sandblasted large thread acid etched titanium implants
Treatment:
Other: sandblasted large acid itched coated titanium implant

Trial contacts and locations

1

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Central trial contact

Mohamed Ha Mahmoud Ismail, PhD

Data sourced from clinicaltrials.gov

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