About this trial
This double-blind, single-center, split-mouth, randomized prospective clinical trial was conducted among 48 systemically and periodontally healthy patients who had bilaterally asymptomatic mandibular third molars.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients who met the requirements of the study, such as attending follow-up sessions and signing the informed consent. 2. Patients with bilateral mandibular asymptomatic vertical third molar teeth with impaction of Class I, level C.22 3. Patients who did not have any significant medical diseases or drug use, were not pregnant, had no allergy, and did not smoke.
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Surgical extraction
Procedure/Surgerysaline irrigation at different temperatures
saline irrigations
Procedure/Surgerysaline irrigation done after 3rd molar surgery
Treatment groups
Trial outcomes
Primary outcomes
post operative pain after 3rd molar surgery
Trismus and swelling were evaluated on the 1st, 3rd, and 7th days postoperatively. Pain perception by visual analog scale (VAS) and the total number of analgesics taken during the 7 postoperative days were recorded
Sponsors and contacts
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