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Determining the Presence of RAP in Orthognathic Patients and Its Effect on Root Resorption by Biomarkers

B

Bezmialem Vakif University

Status

Completed

Conditions

Class III Malocclusion
Root Resorption

Treatments

Procedure: Orthognathic Surgery

Study type

Observational

Funder types

Other

Identifiers

NCT04823325
bkilic001

Details and patient eligibility

About

A prospective clinical trial to what extent inflammatory biomarkers are affected by the medication after orthognathic surgery in early surgical cases and whether these biomarkers affects the amount of maxillary or mandibular incisor root resorption.

Full description

To conduct a prospective clinical trial to what extent inflammatory biomarkers such as OPG, RANKL, IL-1, IL-6, and CRP are affected by the medication after orthognathic surgery in early surgical cases and whether these biomarkers affects the amount of maxillary or mandibular incisor root resorption.

Enrollment

13 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  1. Have skeletal Cl III malocclusion
  2. Wisdom teeth are absent or extracted at least 6 months before the surgery
  3. Need of orthognathic surgery through Le Fort I osteotomy of the maxilla and bilateral sagittal split osteotomies (BSSO) of the mandible.
  4. Undergo fixed orthodontic treatment before and after the orthognathic surgery
  5. Have available orthopantomograms with adequate quality
  6. Have healthy periodontal tissue without inflammation or bleeding before and after the surgery.
  7. Maintain the same medication protocol during and after the surgery.

Exclusion Criteria:

  1. ongoing use of regular medication
  2. smoking
  3. known penicillin allergy,
  4. any immune disorder,
  5. musculoskeletal diseases,
  6. syndromes,
  7. cleft lip-palate,
  8. systemic diseases affecting root resorption,
  9. periodontal and gingival disorders,
  10. missing teeth among upper or lower incisors,
  11. poor oral hygiene.

Trial design

13 participants in 1 patient group

Surgery patients
Description:
Otherwise healthy patients with Skeletal Class III problem
Treatment:
Procedure: Orthognathic Surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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