Evaluation of the Effect of Tea Tree and Chlorhexidine Mouthwashes on Healing After Third Molar Extraction

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorHarran University

About this trial

The purpose of this clinical study is to compare the effects of mouthwashes containing Chlorhexidine and tea tree oil on edema, pain, and trismus after the extraction of impacted third molars. Additionally, the effects on periodontal health will be examined by comparing the gum healing processes of patients using both mouthwashes.The main questions it aims to answer are:

1. Tea tree oil, said to have anti-inflammatory and antibacterial effects, could be an alternative to chlorhexidine in reducing postoperative complications after impacted tooth extraction. 2. Does tea tree oil, which has antimicrobial effects, have as positive an impact on periodontal health as chlorhexidine?Researchers will compare tea tree oil to chlorhexidine (routinely prescribed after the extraction of an impacted wisdom tooth) to see if tea tree oil works to decrease postoperative complications.

Participants will:

For 7 days after the operation, they will gargle with chlorhexidine mouthwash or mouthwash containing tea tree oil 3 times a day. They will come to the clinic for check-ups and measurements on the 2nd and 7th days after the operation. They will record their pain levels and the number of painkillers they take daily.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Individuals undergoing extraction of Class 2, Class B mandibular third molars impacted in the lower jaw (Pell & Gregory).

Individuals aged 18-65.

Individuals must be in stable general health (e.g., free of serious cardiovascular or kidney disease).

Individuals willing to use tea tree extract or other treatments.

Disqualifiers

Individuals with a known allergy or hypersensitivity to tea tree extract.

Individuals with serious illnesses such as heart failure or kidney disease. Patients with bleeding disorders.

Individuals during pregnancy and breastfeeding.

Individuals taking medications that may interact with tea tree extract (e.g., blood thinners or antihypertensives)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Chlorhexidine Gluconate 0.12% Mouthwash

    Drug

    Participants will be prescribed to gargle with chlorhexidine, which is the routine recommendation after brushing their teeth 3 times a day for 7 days after the impacted tooth extraction.

  • Tea Tree Oil mouthwash

    Drug

    Participants will be prescribed to gargle with tea tree oil-containing water after brushing their teeth three times a day for 7 days following the extraction of an impacted tooth.

Treatment groups

54 Participants
are divided into 2 treatment groups
Group A: chlorhexidine groupActive comparator 1 intervention
Group B: tea tree oil groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

pain VAS measurement

The patient will be given a chart with a 7-day VAS scale for pain control after tooth extraction. They will be asked to record their pain daily on a scale of 0 (no pain) to 10 (the worst imaginable pain) for 7 days, and to note how many painkillers they used.

Time frame
preoperative, postoperative day 2, post operative day 7
2

amount of mouth opening

Restriction in mouth opening for 7 days after impacted tooth extraction surgery

Time frame
preoperative, postoperative day 2, post operative day 7
3

distance from the angulus to the labial commissure, external eye angle, tragus, pogonion, and nasal line

The amount of facial swelling during the 7 days following impacted tooth extraction surgery

Time frame
preoperative, postoperative day 2, post operative day 7

Secondary outcomes

1

Pocket depth measurement of the second molar tooth next to the extraction site and assessment of plaque presence

The level of periodontal healing of teeth in the adjacent area during the 7 days following impacted tooth extraction surgery

Time frame
preoperative, postoperative day 2, post operative day 7

Other outcomes

Sponsors and contacts

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