Antibiotic Efficacy in Third Molar Surgery

This study has been completed.
Sponsor:
Collaborator:
Oral and Maxillofacial Surgery Foundation, Rosemont ,Illinois
Information provided by:
Massachusetts General Hospital
ClinicalTrials.gov Identifier:
NCT00118820
First received: July 1, 2005
Last updated: July 14, 2010
Last verified: July 2010
  Purpose

Despite over 50 years of antibiotic use and multiple clinical investigations (>50), no definitive studies exist to confirm or refute the use of systemic antibiotics to prevent postoperative inflammatory complications after third molar (M3), aka "wisdom teeth" removal. Among patients having M3s extracted, does the administration of systemic prophylactic antibiotics when compared to placebo, decrease the rate of postoperative inflammatory complications? The first specific aim of the study is to implement a randomized, placebo-controlled clinical trial to determine if systemic prophylactic antibiotics, when compared to placebo, decrease the rate of postoperative alveolar osteitis (AO) after M3 extraction. For this proposal, postoperative AO is the primary outcome variable.

The second specific aim is to implement a pilot study using a randomized, placebo-controlled clinical trial to determine if systemic prophylactic antibiotics, when compared to placebo, decrease the rate of postoperative infection after M3 extraction. For the purposes of this proposal, postoperative infection is a secondary outcome variable. Based on sample size estimates, we believe it will be necessary to implement a multi-year trial to address the second specific aim definitively. As such, we will use the experience and preliminary results derived from this clinical trial to develop and implement a future large scale clinical trial.

The third specific aim is to identify risk factors associated with postoperative inflammatory complications in order to develop a model to predict if the prophylactic administration of antibiotics will prevent the postoperative inflammatory complications of alveolar osteitis and infection following the removal of M3's.

The long-term goal of this project is to provide compelling clinical evidence to support recommendations regarding the use of systemic antibiotics in this setting and alter clinical practice based on the results of a well-done, definitive clinical investigation.


Condition Intervention Phase
Alveolar Osteitis
Dry Socket
Infection
Drug: IV Preoperative antibiotic or placebo
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: Antibiotic Efficacy in Third Molar Surgery

Resource links provided by NLM:


Further study details as provided by Massachusetts General Hospital:

Primary Outcome Measures:
  • Presence or absence of postoperative inflammatory complication: i.e., alveolar osteitis or infection

Secondary Outcome Measures:
  • Adverse effects from treatment: i.e., antibiotic administration

Estimated Enrollment: 132
Study Start Date: March 2004
Study Completion Date: June 2006
Primary Completion Date: June 2006 (Final data collection date for primary outcome measure)
Detailed Description:

The management of impacted M3s is a high volume procedure. In the United States, the cost of M3 removal has been estimated to be over 2 billion dollars, not including costs for consults, x-rays, medications, surgical center charges, or over 5 million surgical extractions and treatment of postoperative inflammatory complications (Flick. 1999). Practices associated with M3 removal can have a significant impact on large numbers of patients, providers, and payers. There is currently no consensus on the use of systemic antibiotic prophylaxis to decrease the risk of inflammatory complications following M3 removal.The most common post-operative inflammatory complications following M3 extraction are alveolar osteitis (AO) and wound infection (Larsen, 1992; Piecuch et al., 1995; Sekar et al., 2001). AO, aka "dry socket," is a wound-healing problem characterized by severe, unremitting pain. The reported frequency of AO is 6-68%. Bacterial colonization stimulates plasmin production and fibrinolysis with dissolution of the extraction site clot . More than 45% of patients who sustain AO require 4 or 5 more postoperative appointments for resolution of symptoms (Larsen, 1992; Andra et al., 1990). Given its common occurrence, identifying treatments, i.e. systemic antibiotics, to decrease the rate of AO following M3 extraction would be an important contribution to enhancing patient outcomes. The second common postoperative inflammatory condition following M3 extraction is wound infection. The reported frequency of postoperative infection ranges from 1.2 - 27%, with most studies reporting a frequency of <10%. Because wound infections are bacterial, it is hypothesized that using systemic antibiotics will reduce the rate of postoperative wound infections. There are, however, no definitive prospective studies that support or refute the necessity of systemic antibiotics in the prevention of postoperative inflammatory complications of AO or infection.

All studies published to date addressing the role of systemic antibiotics and M3 removal have one or more major methodological flaws in study design characterized as :1) no or ambiguous definition of the outcome variable, 2) inadequate sample size, 3) non-uniformity of protocol design, 4) lack of randomization techniques and 5) poor-follow-up monitoring. Clearly, there is a need for a definitive, rigorous, well-designed placebo-controlled randomized clinical trial to ascertain the efficacy of systemic antibiotics in preventing postoperative inflammatory complications after M3 removal.

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  Eligibility

Ages Eligible for Study:   13 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Demographics: While all ages are eligible for study enrollment, as a practical matter, most patients having M3s removed are usually > 13-14 years of age.
  • Gender: Males and females will be offered to participate in this study.
  • Race: All races and ethnicities are eligible for study enrollment.
  • Clinical status: at least one impacted mandibular third molar ( M3 ) must be scheduled for extraction.
  • Anesthesia: Patient request that the procedure be executed using intravenous sedation or general anesthesia. Intravenous sedation will be accomplished with use of an IV placed in the antecubital fossa of each patient
  • Health status: Healthy patients or patients with mild systemic disease, i.e. ASA status < 3, are eligible for study enrollment.

Exclusion Criteria:

  • Pre-existing infection: Infection is characterised as having an area with frank purulence and/or cellulitis characterized by erythema, induration and inability to open the mouth wide enough to provide access to the airway.
  • Pre-existing Systemic Illness: as evidenced by severe dry mouth, patients who have undergone radiotherapy for oral cancer, patients that are immunocompromised, patients that require antibiotic prophylaxis for endocarditis, as well as, patients who are taking antimicrobials for other systemic diseases, i.e., uncontrolled diabetes., ASA status > 2.
  • Allergic Reactions to Medications: Patients who are allergic to Penicillin and Clindamycin will be excluded from the study.
  • Anesthesia: Patient request that the operation be performed with local anesthesia without intravenous sedation or general anesthesia.
  • Pregnancy: Pregnancy is a relative contraindication for study enrollment. If after consultation with the obstetrician, there is no contraindication to removing the impacted teeth with sedation or contraindication to receiving the test medications (penicillin or clindamycin) and the patient wants to pursue treatment, she would be considered eligible for study enrollment.
  Contacts and Locations
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00118820

Locations
United States, Massachusetts
Outpatient Clinic for Oral and Maxillofacial Surgery, Wang Pavilion, ACC230
Boston, Massachusetts, United States, 02114
Sponsors and Collaborators
Massachusetts General Hospital
Oral and Maxillofacial Surgery Foundation, Rosemont ,Illinois
Investigators
Principal Investigator: Thomas B Dodson, DMD,MPH Massachusetts General Hospital
Principal Investigator: Leslie R Halpern, DDS,MD,MPH Massachusetts General Hospital
  More Information

No publications provided

Responsible Party: Leslie Halpern, DDS, MD, Massachusetts General Hospital
ClinicalTrials.gov Identifier: NCT00118820     History of Changes
Other Study ID Numbers: 2002-P000048/11
Study First Received: July 1, 2005
Last Updated: July 14, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by Massachusetts General Hospital:
Dry socket
Third molar
Infection
postop-infection
Antibiotic efficacy
Infection characterized by pus,erythema,edema and pain

Additional relevant MeSH terms:
Dry Socket
Osteitis
Mouth Diseases
Stomatognathic Diseases
Bone Diseases, Infectious
Infection
Bone Diseases
Musculoskeletal Diseases
Anti-Bacterial Agents
Antibiotics, Antitubercular
Anti-Infective Agents
Therapeutic Uses
Pharmacologic Actions
Antitubercular Agents

ClinicalTrials.gov processed this record on August 21, 2014