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Acute Inflammation After Wisdom Tooth Removal

Not Applicable
Completed
Conditions
Tooth Impacted
Interventions
Procedure: Wisdom tooth removal
Registration Number
NCT03048175
Lead Sponsor
University of Pisa
Brief Summary

Third molar (wisdom teeth) extraction is one of the most frequent intervention in dentistry. Nevertheless, little is known about the level of general body inflammation of subjects with impacted or semi-impacted third molars. Moreover, The possible effects of surgical removal of wisdom teeth on the overall health are not known.

Thus, a study in which 40 subjects has been designed. Twenty subjects were affected by bilateral wisdom tooth pathology necessitating for extraction of both teeth. Control group comprised 20 subjects with absence of wisdom teeth or completely erupted wisdom teeth without pathology associated to or history of previous extraction of both wisdom teeth.

In both groups a medical and dental examination will be performed at the baseline and 3 months after baseline for the control group or after the second third molar extraction in the control group. Blood will be also withdrawn to assess systemic inflammation and other systemic parameters.

Parameter were evaluated via high sensitive c reactive protein (CRP), lipids, fibrinogen, oxidative stress and endothelial function analysis.

Detailed Description

Third molar extraction is one of the most frequent intervention in dentistry. Nevertheless, little is known about the systemic aspect of subjects with impacted or semi-impacted third molars and the possible effects of surgical removal on their systemic parameters. A case-control study of 40 subjects has been designed to evaluate i) the overall systemic inflammation and metabolism of subjects with bilateral third molars compared to subjects with no third molars and ii) the effect of bilateral removal in the immediate and medium postsurgical period. Systemic parameters are evaluated via high sensitive c reactive protein (CRP), lipids, fibrinogen, oxidative stress and endothelial function analysis.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • cases: bilateral wisdom tooth pathology.
  • control: agenesia/previous extraction/no symptoms of the lower third molars.
Exclusion Criteria
  • younger than 18 years and older than 65 years;
  • pregnant or lactating females;
  • females using contraceptive methods;
  • suffering from any systemic illness;
  • undergoing any pharmacological treatment within 30 days prior to the inclusion
  • patients affected by periodontal disease (radiographic diagnosis of vertical bone defects or bone resorption equal to 20% of the root length);
  • patients with periapical and periradicular radiolucent areas X-ray detectable;
  • patients unable to participate to study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cases: wisdom tooth pathologyWisdom tooth removalSubjects affected by bilateral wisdom tooth pathology, undergoing surgical removal
Primary Outcome Measures
NameTimeMethod
Changes in C-reactive protein (CRP)baseline, 24 and three months after the second extraction

High-Sensitive plasmatic C-reactive protein

Secondary Outcome Measures
NameTimeMethod
Changes in plasma malondialdehyde (MDA)baseline, 24 and three months after the second extraction

plasma malondialdehyde

Changes in lipoperoxides (LOOH)baseline, 24 and three months after the second extraction

lipoperoxides levels in plasma

Changes in ferric-reducing antioxidant power (FRAP)baseline, 24 and three months after the second extraction

FRAP levels in plasma

Changes in endothelial flow-mediated dilation (FMD) calculated as maximal percentual increase in diameter of the blood vessel above baselinebaseline, 24 and three months after the second extraction

Endothelium-dependent response of the brachial artery in response to increased blood flow by high resolution ultrasound with a 7.5 MHz linear array transducer

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