NCT06561282

Brief Summary

The aim of this observational study is to investigate the role of the glucose-potassium ratio in predicting mortality in patients with major burn trauma. The main question it aims to answer is: Can the glucose-potassium ratio predict mortality in major burn patients? The glucose-to-potassium ratios of major burn patients at the time of initial hospitalization will be determined, and their relationship with mortality will be analyzed.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2022

Typical duration for all trials

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2022

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 17, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 20, 2024

Completed
Last Updated

August 21, 2024

Status Verified

August 1, 2024

Enrollment Period

2 years

First QC Date

August 17, 2024

Last Update Submit

August 19, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Glucose-to-potassium ratio

    The glucose-to-potassium ratio is calculated by dividing the participants' glucose values when they first apply to the hospital by their potassium values.

    2 days

Secondary Outcomes (4)

  • Female/Male ratio

    2 days

  • Mean percent of total body surface area burned

    2 days

  • Burn infection rate

    2 days

  • Mortality rate

    2 days

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consisted of patients of all age groups who were admitted to the burn center between May 2022 and May 2024 with 2nd degree and deeper burns of 40% and above total burn surface area, 3rd and 4th degree burns of 20% and above total burn surface area, and inhalation burns. Patients with missing data, patients with burn trauma of more than 24 hours since the onset of burn trauma, 1st degree burns, patients with diabetes mellitus or renal failure, and patients using potassium-regulating drugs were excluded from the study.

You may qualify if:

  • All burns \>40% of total body surface area (2nd degree or deeper)
  • Burns with inhalation injury
  • Burns \>20% of total body surface area 3nd degree or deeper

You may not qualify if:

  • First degree burns
  • Patients have more than 24 hours since the onset of burn trauma
  • Patients with diabetes mellitus
  • Patients with chronic renal failure
  • Patients taking potassium-modifying medication
  • Patients with missing data

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Konya Training and Research Hospital

Konya, 42090, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Burns

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Officials

  • Alpaslan Sahin, Assoc. Prof.

    Principal Investigator

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

August 17, 2024

First Posted

August 20, 2024

Study Start

May 1, 2022

Primary Completion

May 1, 2024

Study Completion

July 1, 2024

Last Updated

August 21, 2024

Record last verified: 2024-08

Locations