EFFECT OF ENDOTRACHEAL TUBE DETECTION ON PRESSURE

Marmara University Pendik Training and Research Hospital

Status: Completed

Conditions: Pressure Injury

Treatments: Other: BANDAGE; Other: ENDOTRAKEAL TUBE HOLDER

Study type: Interventional

Funder types: Other

Identifiers

NCT05142579

Marmara EAH-ALEV GENÇ

Details and patient eligibility

About

This study was conducted to examine the effect of two different tube detection on pressure wound formation in the intensive care unit. The search was carried out with a total of 60 patients that 30 of 60 them are interventions and 30 of 60 as experiments, who were hospitalized in the anesthesia and reanimation intensive care unit of an Educational Research Hospital. The 60 patients who made up the sample were assigned 2 groups using a computer program that produced random numbers. For the purpose of the study, the groups were encoded as groups A and B, and each group was tested with two different endotracheal tube detection methods which was applied to the patients in the groups. Data from the study were collected using the introductory and clinical features form, the braden pressure wound risk diagnostic scale, the pressure ulcer recovery assessment scale, the international pressure wound staging system, and the eilers oral assessment guide. Patients in both groups were monitored for four days for oral presure injury. During this process, the tube detection of both groups was changed every 24 hours, and the tubes were repositioned every 4 hours. At the end of the fourth day, wound assesments of patients who developed pressure wounds were performed by using the international pressure staging system and the pressure ulcer recovery assessment scale. Relatives of the patients who were scheduled to conduct the study were informed about the study by oral and written and their consent was obtained.

Enrollment: 60 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Must be between the ages of 18-65
• Must be intubated oratraceal

Exclusion criteria

• Oral pressure wounds
• Burns on the face
• Diabetes
• Facial and neck trauma

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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60 participants in 2 patient groups

ENDOTRACHEAL TUBE HOLDER

Experimental group

Description:

Endotracheal tube holder was used for endotracheal tube detection of patients in this group.

Treatment:

Other: ENDOTRAKEAL TUBE HOLDER

BANDAGE

Active Comparator group

Description:

The bandage was used for endotracheal tube detection of patients in this group.

Treatment:

Other: BANDAGE