跳至主要内容
临床试验/NCT07635225
NCT07635225已完成不适用

Investigating the Effect of Oral Care Frequency on Oral Mucosal Tissue Integrity in Critically Ill Patients.

Balikesir University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年8月20日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1

研究概览

简要总结

This study aims to investigate the effect of oral care frequency on oral mucosal tissue integrity in intensive care patients.

详细描述

Research data will be collected from the Adult Intensive Care Units of Balıkesir University Health Practice and Research Hospital. Patients meeting the inclusion criteria will be informed about the research, and those who volunteer to participate, or their relatives, will provide written/verbal consent using an Informed Consent Form. The assignment of patients to different groups will be determined using simple randomization on the randomizer.org website. Patients admitted to the intensive care unit at the start of the study will be assigned to control and intervention groups according to the numbers on the randomizer.org website. Oral care swabs will be prepared for each patient in both the control and intervention groups, with four swabs per patient, moistened with a 0.25% chlorhexidine gluconate solution. If the patient is conscious, they will be placed in a comfortable position; if unconscious, their head will be positioned sideways towards the person performing the procedure. Oral care will be performed on the patient, covering all teeth, inner cheeks, under the tongue, gums, and other soft tissues. After the patient's oral care procedure is complete, the patient will be returned to their original position, and the procedure will be finished. Each care session will last at least 2 minutes. Patients in the control group will receive oral care four times a day, every six hours. Patients in the intervention group will receive oral care at a frequency determined individually based on their scores on the intensive care oral care frequency assessment scale. Patients in both groups will be evaluated at the beginning and throughout the intervention using the oral mucosa assessment scale to assess the effect of the oral care on the oral mucosa. The intervention is planned to continue for five days, and the results will be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Months 至 95 Months(Child)
性别
All
接受健康志愿者

入选标准

  • •Patients admitted to the adult intensive care unit:
  • Patients aged 18 and over
  • Patients who agreed to participate in the study (voluntary informed consent obtained from the patient or their relatives)
  • Patients who are not allergic to the contents of the oral care solution to be used were included in the study.

排除标准

  • • Patients under 18 years of age
  • Patients with oral bleeding
  • Patients with thrombocytopenia
  • Patients who have undergone oral surgery
  • Patients who did not consent to the study (either from the patient themselves or a relative) were not included in the study.

研究者

发起方
Balikesir University
申办方类型
Other
责任方
Principal Investigator
主要研究者

berat fidan

nurse

Balikesir University

研究点 (1)

Loading locations...

相似试验