Analysis of the Effects of Preoperative Mouthwash Intervention on the Microbiome,Tumor Immune Environment,and Prognosis in Oral Cancer

Not provided0 sites100 target enrollmentStarted: TBD

Conditions

Trial Snapshot

No summary available.

•1.Age 18 years or older at the time of consent.
•2.Ability to tolerate oral intake.
•3.Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, defined as follows:
•0: Fully active, able to carry on all pre-disease activities without restriction.
•1: Restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature.
•4.Provision of written informed consent by the participant after receiving a full explanation of the study.

•1.Presence of an active infection requiring systemic treatment.
•2.Women who are pregnant, potentially pregnant, or breastfeeding.
•3.Presence of psychiatric disorders or psychiatric symptoms that, in the opinion of the investigator, would interfere with participation in the study.
•4.Evidence of active bleeding.
•5.Ongoing systemic corticosteroid therapy or treatment with immunosuppressive agents.
•6.Use of systemic antibiotics within 1 week prior to surgery (in principle).
•7.Participation in another interventional clinical study.
•8.Any other condition that, in the judgment of the principal investigator or sub-investigator, renders the participant unsuitable for the study.

Sponsor

Not provided