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therapy antiedemigena through administration of corticosteroidi after surgical extraction of the teeth of the judgment. - ND

Conditions
This study is going to be performed on patients afferent to the service of Chirurgia Maxillo Facciale dell’Ospedale Maggiore della Carita` di Novara subject to eights bony included extraction.
MedDRA version: 9.1Level: SOCClassification code 10042613
Registration Number
EUCTR2010-021295-28-IT
Lead Sponsor
AZIENDA OSPEDALIERA MAGGIORE DELLA CARITA` DI NOVARA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1.patients anti-edema therapy with systemic intravenous corticosteroids administered.
2.patients anti-edema therapy with systemic oral corticosteroids administered.
3.patients anti-edema therapy with local corticosteroids
Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Presence of acute oral pathology (periodontitis, perichondropathy, abscesses, mucositis etc..),
Chronic oral pathology causing flogosis,
Patients treated for acute oral pathology (abscesses) till 2 weeks from regression of the event or non regressing by 1? level medical therapy (oral antibiotic therapy),
Post-operative local complications and/or extension of hospitalization for any reason,
Systemic patholgies:
•severe internistic pathologies (systemic infectious deseases, cardiovascular patholgies, liver deseases, hemopathies, coagulation deficiency, diabetes, cancer), or pre-hospitalization blood exams altered ( ex. Creatinine > 1.5mg/dl),
•recent anti-nflammatory therapy
•chronic use of such drugs may alter inflammatory response (antihistamines, steroids, antidepressants, NSAIDS),
Pregnancy and nursing,
Surgical procedures total time: all the patients surgically treated over 60’ minutes have been excluded.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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