Investigation of the Effect of Blood Pressure on Bedsores
1 other identifier
observational
148
1 country
1
Brief Summary
The aim of this study is to comprehensively investigate the effect of blood pressure levels on the development of bedsores (pressure ulcers) in adult patients hospitalized in the internal medicine intensive care unit.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2026
Shorter than P25 for all trials
1 active site
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
First Submitted
Initial submission to the registry
June 24, 2026
CompletedFirst Posted
Study publicly available on registry
July 10, 2026
CompletedStudy Start
First participant enrolled
July 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 20, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 20, 2026
July 13, 2026
July 1, 2026
4 months
June 24, 2026
July 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Decubitus Ulcer
Pressure ulcers will be assessed using the Norton Pressure Ulcer Scale Daily Rating.
For 10 days
Secondary Outcomes (3)
Vital signs - Blood pressure measurements (SBP, DBP)
For 10 days
Vital signs - heart rate
For 10 days
Vital signs - respiratory rate
For 10 days
Study Arms (1)
Intensive care patients
The development and timing of bedsores in patients will be recorded. Vital signs will also be monitored.
Eligibility Criteria
SBU. Van Education and Research Hospital Internal Intensive Care Unit
You may qualify if:
- Patients admitted to the intensive care unit,
- Aged between 18-70 years,
- Bedridden, immobile patients,
- Patients who have signed the informed consent form themselves or through a close relative.
You may not qualify if:
- Patients under 18 years of age,
- Patients who did not give their consent for the study or whose relatives did not consent, or who wanted to leave while the study was ongoing,
- Patients who arrived with bedsores
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
SBU. Van Education and Research Hospital
Van, 65000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
yavuz üren
Yuzuncu Yil University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst.Prof.
Study Record Dates
First Submitted
June 24, 2026
First Posted
July 10, 2026
Study Start
July 10, 2026
Primary Completion (Estimated)
November 20, 2026
Study Completion (Estimated)
November 20, 2026
Last Updated
July 13, 2026
Record last verified: 2026-07