Comparing the effect of Ortodentol and chlorhexidine mouthwashes 10% and /12 percent on oral hygiene intubated patients in intensive care units

Not Applicable

• Conditions: Condition 1: Chronic Obstruactive Pulmanary Disease. Condition 2: Diabeteic Mellitus. Condition 3: Respiratory Distress Syndrome. Condition 4: Multiple Truma. Condition 5: Cerebral Vascular Attacke. Condition 6: Gastrointestinal haemorrhage. Condition 7: Poisoning. Condition 8: laparatomy. Condition 9: Intracerebral haemorrhage.; Chronic obstructive pulmonary disease, unspecified; Diabetes mellitus; Adult respiratory distress syndrome; Injuries involving multiple body regions; Stroke, not specified as haemorrhage or infarction; Gastrointestinal haemorrhage, unspecified; Sequelae of poisoning by drugs, medicaments and biological substances; Unintentional cut, puncture, perforation or haemorrhage during surgical and medical care; Sequelae of cerebrovascular disease

• Registration Number: IRCT2017012232101N1
• Lead Sponsor: Vice , President , Research and Technology , University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Inclusion criteria included: the patient has an endotracheal tube through the mouth ;with the age of 15-85 years ; 8 hours of intubation in the intensive care unit, before ; no history of allergy is to plant compounds Savory (carvacrol) ; Lack of any damage characterized by endotracheal intubation or planes in the mouth Lesion is unknown.

Exclusion criteria included: transmission or discharge or death of the patient from the intensive care unit before the study was completed ; Creating profit any damage characterized by endotracheal intubation or planes or other physical Hram ; Lack of desire to continue to study the patient's legal guardian ; and immune system dysfunction, radiotherapy and chemotherapy and having any malignant disease.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Oral Health. Timepoint: Before and after the intervention. Method of measurement: Beck standard questionnaire and measured plaque and oral mucosal.

Secondary Outcome Measures

Name	Time	Method
Malnutrition. Timepoint: Scale. Method of measurement: Relative.;Side Efect. Timepoint: Scale. Method of measurement: Relative.