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Effect of Oral Preparation on Bacterial Colonization of the Pharyngeal Mucosa in Surgery of Head and Neck Cancer

Effect of Oral Preparation on Bacterial Colonization of the Pharyngeal Mucosa in Surgery of Head and Neck Cancer

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02753387
Acronym
ORAL-ISO
Enrollment
80
Registered
2016-04-27
Start date
2016-05-23
Completion date
2018-09-05
Last updated
2018-12-20

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

Conditions

Bacterial Infection

Keywords

mouthwash, head and neck cancer, chlorhexidine, pathogens germs

Brief summary

Surgical site infections are an important health indicator for hospitals and a significant medico-economic issue. The aim of the study is to assess the impact of chlorhexidine mouthwash performed before surgery on the bacterial colonization of the pharyngeal mucosa.

Detailed description

The main objective is to reduce the number of patients with significant pathogenic bacterial colonization for pharyngeal mucosa at the end of the surgery. Oral flora is the same as the pharyngeal flora, so this suggests that the action of the oral mouthwash may also act in pharyngeal mucosa by buccopharyngeal communication. Patients will be randomized into two groups : * preoperative oral preparation with sodium chloride (NaCl) 0.9% (control group) * preoperative oral preparation with chlorhexidine (experimental group) A quantitative and qualitative analysis will be performed from samples collected during the surgery : before mouthwash (T0), after mouthwash (T1), before intubation in the operating room (T2), after intubation (T3), before incision (T4) and just before the end of the intervention on the mucosal scar (T5)

Interventions

DRUGChlorhexidine

4 mouthwashes during 30 seconds with Eludril Perio 10 ml and 1 application after intubation with Eludril Perio

4 mouthwashes during 30 seconds with NaCl 0.9 % 10 ml and 1 application after intubation with NaCl 0.9 %

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Histological evidence of cancer regardless of histological type * Surgical treatment requiring mucosal effraction regardless of the surgical approach; * Patient over 18 years old; * Oral cancer, oropharyngeal cancer, hypopharyngeal cancer or laryngeal cancer; * Written and informed patient consent

Exclusion criteria

* Concomitant Vascular Interventions; * Interventional radiology; * Needing of second surgery at a same location during the 30 postoperative days); * Cancer of the paranasal sinus, nasal cavity, skull base, salivary glands, skin, * Neck dissection without mucosal effraction * Thyroid or parathyroid surgery * Size tumor forbidden tumor surgery * Allergy to any tested product; * Concurrent infection the day before or day of surgery * Protected adults (guardianship) and persons deprived of liberty

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients with pharyngeal mucosa colonization (>=10^2 Colony Forming Unit (CFU)/ml of pathogen germs of the oral flora) at the end of the surgeryThe day of the surgeryThe percentage of patients with pharyngeal mucosa colonization will be determined from the sample collected on the mucosal scar just before the end of the surgery (T5)

Secondary

MeasureTime frameDescription
Type of oral germsThe day of the surgeryThe type of germs will be determined for all the samples collected during the surgery (i.e. before mouthwash (T0), after mouthwash (T1), before intubation in the operating room (T2), after intubation (T3), before incision (T4) and just before the end of the intervention on the mucosal scar (T5))
Number of positive cultures of pathogen germsThe day of the surgeryThe number of positive cultures of pathogen germs will be determined for all the samples collected during the surgery (i.e. before mouthwash (T0), after mouthwash (T1), before intubation in the operating room (T2), after intubation (T3), before incision (T4) and just before the end of the intervention on the mucosal scar (T5))
Kinetics of the number of CFU/mlThe day of the surgeryThe kinetics of the number of CFU/ml will be determined from all the samples collected during the surgery (i.e. before mouthwash (T0), after mouthwash (T1), before intubation in the operating room (T2), after intubation (T3), before incision (T4) and just before the end of the intervention on the mucosal scar (T5))
Number of patients with a significant rate of pathogen germs (>=10^2 CFU/ml) at T1The day of the surgeryThe number of patients with a significant rate of pathogen germs will be determined from the sample collected after mouthwash (T1)
Surgical site infections rate in the postoperative month (standard definition of the Centers for Disease Control and Prevention, Atlanta)30 days
Number of patients who processed correctly preoperative mouthwashThe day of the surgery
Change in the number of CFU/ml of pathogen germs before and after intubation (T2-T3)The day of the surgeryThe change in the number of CFU/ml of pathogen germs will be assessed using the samples collected before (T2) and after intubation (T3)
Number of CFU/ml of pathogens germsThe day of the surgeryThe number of CFU/ml of pathogens germs will be determined for all the samples collected during the surgery (i.e. before mouthwash (T0), after mouthwash (T1), before intubation in the operating room (T2), after intubation (T3), before incision (T4) and just before the end of the intervention on the mucosal scar (T5))

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026