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Completed

NCT Number: NCT05403099

Effect of Topical Application of Hyaluronic Acid on Stability of Immediate Loading Dental Implant in Posterior Maxilla

Effect of Topical Application of Hyaluronic Acid on Stability of Immediate Loading Dental Implant in Posterior Maxilla

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Key information

Conditions

Missing Teeth Anodontia Congenital Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities Stomatognathic Diseases Stomatognathic System Abnormalities Tooth Abnormalities Tooth Diseases

Age range

20 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Merna Elhadidi

Al Mansurah, Egypt

About this study

Patients were randomly divided into two groups:

Group I (Control group):

Ten implants were placed in posterior maxilla and immediately loaded.

Group II (Study group):

Ten implants were coated with HA before placement in posterior maxilla and immediately loaded.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Highly motivated patients with good oral hygiene.
  • Age 18 years or older.
  • Adequate alveolar bone volume at the implant site, at least 6mm in width and 15 mm in height.
  • Free from any parafunctional habits

Exclusion criteria

  • Patients suffering from any systemic or local disease that contraindicate implant placement or surgery.
  • Pregnancy.
  • Smokers.

Treatment and study plan

Hyaluronic acid

Other

immediate placement of dental implant after topical application of hyaluronic acid on implant surface

conventional implant placement

Other

immediate placement of dental implant without application of hyaluronic acid on implant surface

Primary outcomes

  1. implant stability

    Time frame: immediately after surgery

    using radiofrequency analysis

  2. implant stability

    Time frame: one month

    using radiofrequency analysis

  3. implant stability

    Time frame: three months

    using radiofrequency analysis

  4. implant stability

    Time frame: six months

    using radiofrequency analysis

  5. bone density

    Time frame: three months

    bone density around the implant is measured in cone beam computed tomography

Secondary outcomes

  1. propping depth

    Time frame: six months

    The distance between the gingival margin and the base of the pocket

  2. bleeding inex

    Time frame: six months

    Modified sulcus bleeding index

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jun 3, 2022
Registry last updated
Jun 3, 2022

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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