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Clinical Trials/ISRCTN14639952
ISRCTN14639952Active, not recruitingUnknown

Evaluation of the efficacy of topical ozonated olive oil gel on socket healing after surgical extraction of impacted mandibular third molars

Damascus University0 sites18 target enrollmentStarted: May 22, 2023Last updated:
Conditions

Trial Snapshot

Phase
Unknown
Status
Active, not recruiting
Enrollment
18

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
All

Inclusion Criteria

  • 1. Aged between 18 - 35 years old
  • 2. Patients with symmetrically impacted mandibular third molar on both sides and of the same classification according to Pell & Gregory
  • 3. Classification of general health status: ASA I (a normal, healthy, non-smoking patient with a normal body mass index) (American Society of Anesthesiologists, 2020)
  • 4. Patients who are cooperative, have good mental ability and are committed to periodic reviews, postoperative recommendations and oral care
  • 5. No previous surgical treatment of the target area
  • 6. Patients with good oral health and healthy periodontal tissues

Exclusion Criteria

  • 1. Patients with systemic disease affecting wound healing
  • 2. Patients with fungal lesions in oral cavity
  • 3. Presence of a periodontal injury in the lower second molar
  • 4. Psychologically unstable patients
  • 5. Patients who smoke
  • 6. Uncooperative patients
  • 7. The presence of local pathogens around the impacted molars, such as large cysts and tumors
  • 8. The presence of any local or general contraindications to the use of ozonted olive oil gel such as systemic diseases, G6PD deficiency, or a history of allergy, local infection, a pregnant woman or using contraceptive drugs or breastfeeding, as well as recent myocardial infarction
  • 9. Severe anemia
  • 10. Hyperthyroidism

Investigators

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