NCT07688057

Brief Summary

This study was conducted to compare the effects of oral care performed using chlorhexidine (CHX), green tea, and white tea solutions on oral health, functional status, and the development of ventilator-associated pneumonia (VAP) in intensive care unit patients receiving mechanical ventilation (MV)

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
63

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2024

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

June 30, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 7, 2026

Completed
Last Updated

July 8, 2026

Status Verified

July 1, 2026

Enrollment Period

2 years

First QC Date

June 30, 2026

Last Update Submit

July 6, 2026

Conditions

Keywords

VAPOral caregreen teawhite teaclorhexidine

Outcome Measures

Primary Outcomes (1)

  • ventilator associated pneumonia devolopment

    Comparison of the incidence of ventilator-associated pneumonia among the chlorhexidine, green tea, and white tea oral care groups.

    7 days

Study Arms (3)

chlorhexidine group

EXPERIMENTAL

Participants received oral care using chlorhexidine solution according to the study protocol.

Procedure: Clorhexidine group

green tea group

EXPERIMENTAL

Participants received oral care using green tea according to the study protocol.

Procedure: Green Tea group

white tea group

EXPERIMENTAL

Participants received oral care using white tea according to the study protocol.

Procedure: white tea group

Interventions

oral care using clorhexidine solution, green tea and white tea

Also known as: clorhexidine
chlorhexidine group

Participants received oral care using green tea according to the study protocol.

Also known as: green tea
green tea group

Participants received oral care using white tea according to the study protocol.

white tea group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Aged over 18 years
  • With no known allergies
  • Receiving invasive mechanical ventilator support
  • With a negative endotracheal aspirate culture on the day of ICU admission
  • Within the first 24 hours of mechanical ventilator support
  • Patients whose relatives agreed to participate in the study

You may not qualify if:

  • Patients with positive endotracheal aspirate cultures within the first 48 hours of intensive care admission,
  • Patients undergoing radiotherapy or chemotherapy,
  • Patients with contraindications for oral care,
  • Patients with a platelet count below 30,000/mm³,
  • Patients who cannot be positioned appropriately,
  • Patients with agitation severe enough to prevent the procedure from being performed

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Recep Tayyip Erdogan University Research and Training Hospital

Rize, Merkez, 53020, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Tea

Intervention Hierarchy (Ancestors)

Plant PreparationsBiological ProductsComplex MixturesBeveragesDiet, Food, and NutritionPhysiological PhenomenaFood and Beverages

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants were assigned to one of three parallel intervention groups receiving chlorhexidine, green tea, or white tea oral care throughout the study period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Intensive care specialist

Study Record Dates

First Submitted

June 30, 2026

First Posted

July 7, 2026

Study Start

January 1, 2024

Primary Completion

December 31, 2025

Study Completion

April 1, 2026

Last Updated

July 8, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Locations