NCT07696416

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

77
On Track

Trial Health Score

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

Enrollment
148

participants targeted

Target at P50-P75 for all trials

Timeline
3mo left

Started Jul 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress17%
Jul 2026Nov 2026

First Submitted

Initial submission to the registry

June 24, 2026

Completed
16 days until next milestone

First Posted

Study publicly available on registry

July 10, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

July 10, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 20, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 20, 2026

Last Updated

July 13, 2026

Status Verified

July 1, 2026

Enrollment Period

4 months

First QC Date

June 24, 2026

Last Update Submit

July 10, 2026

Conditions

Keywords

Decubitus UlcerBlood pressureİntensive care

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

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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)

RECRUITING

MeSH Terms

Conditions

Pressure Ulcer

Condition Hierarchy (Ancestors)

Skin UlcerSkin DiseasesSkin and Connective Tissue Diseases

Study Officials

  • yavuz üren

    Yuzuncu Yil University

    STUDY CHAIR

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

Locations