Skip to content

Acute Inflammation After Wisdom Tooth Removal

Systemic Inflammation After Wisdom Tooth Removal: a Case-control Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03048175
Acronym
OTTO-SYST
Enrollment
40
Registered
2017-02-09
Start date
2007-04-19
Completion date
2016-06-30
Last updated
2017-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tooth Impacted

Keywords

C-reactive protein, Systemic inflammation, Third molar, Wisdom tooth

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 Blood will be also withdrawn to assess systemic inflammation and other systemic parameters.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.

Interventions

PROCEDUREWisdom tooth removal

After inferior dental and buccal nerve anesthesia a triangular full thickness flap with releasing incision on the mesio-buccal aspect of the second molar is designed. Ostectomy is then performed and tooth is sectioned and gently elevated. Once all the tooth components are extracted, the socket is carefully inspected and flap is sutured with interrupted sutures.

Sponsors

University of Pisa
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Code was assigned to each participant. No info on whether they belong to cases or control was given to researchers and statistician.

Intervention model description

Case-control intervention trial: cases are treated for pathology. Controls do not have pathology.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Changes in C-reactive protein (CRP)baseline, 24 and three months after the second extractionHigh-Sensitive plasmatic C-reactive protein

Secondary

MeasureTime frameDescription
Changes in plasma malondialdehyde (MDA)baseline, 24 and three months after the second extractionplasma malondialdehyde
Changes in lipoperoxides (LOOH)baseline, 24 and three months after the second extractionlipoperoxides levels in plasma
Changes in ferric-reducing antioxidant power (FRAP)baseline, 24 and three months after the second extractionFRAP 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 extractionEndothelium-dependent response of the brachial artery in response to increased blood flow by high resolution ultrasound with a 7.5 MHz linear array transducer

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026