Impact of two types of indwelling catheter in prevention catheter-associated urinary tract infectionson

Comparison of two types of indwelling catheter in prevention catheter-associated urinary tract infections in ICU patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20100816004578N7

Enrollment

Registered

2019-03-14

Start date

2019-04-21

Completion date

Unknown

Last updated

2019-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary tract infection. Other chronic cystitis

Interventions

Intervention 1: Intervention group: In this group of a type of catheter with oval holes on both sides, the LoPro (Low Profile) catheter is a short and an end tip slightly higher than the balloon loop.

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Decreased consciousness (less than 9 in GCS) Normal body temperature (as axillary 35.5-37%) The doctor's order for urinary catheterization Not having a urinary tract infection or bacteriuria prior to admission Not having underlying diseases such as diabetes, CKD, nephrosclerosis, acute or chronic glomerulonephritis, and pyelonephritis Not having immune deficiency disorders such as lupus erythematosus, rheumatoid arthritis, MS Not having trauma and rupture of the urethra and bladder Not getting aminoglycoside medications Age over 18 years

Exclusion criteria

Exclusion criteria: Exit the catheter for any reason (exits by patient or on doctor's instructions) before 3 days Death or transmission of the patient before the completion of the study

Design outcomes

Primary

Measure	Time frame
Number Bacteria. Timepoint: Before and After 1?2?3 days. Method of measurement: Urine Culture.;Type of Bacteria. Timepoint: Before and After 1?2?3 days. Method of measurement: Urine Culture.	—

Secondary

Measure	Time frame
ESR. Timepoint: Before and After 3 days. Method of measurement: Vstrgryn.;Leukocytosis. Timepoint: Before and After 3 days. Method of measurement: Cell Blood Count.;Nitrite. Timepoint: Before and After 1.2.3 days. Method of measurement: Urinalysis.;Body temperature. Timepoint: Before and After 1.2.3 days. Method of measurement: Axillary with medical thermometer.;PH of the urine. Timepoint: Before and After 1.2.3 days. Method of measurement: DIP STICK.;The color of the urine. Timepoint: Before and After 1.2.3 days. Method of measurement: DIP STICK.	—

Measure

Time frame

ESR. Timepoint: Before and After 3 days. Method of measurement: Vstrgryn.;Leukocytosis. Timepoint: Before and After 3 days. Method of measurement: Cell Blood Count.;Nitrite. Timepoint: Before and After 1.2.3 days. Method of measurement: Urinalysis.;Body temperature. Timepoint: Before and After 1.2.3 days. Method of measurement: Axillary with medical thermometer.;PH of the urine. Timepoint: Before and After 1.2.3 days. Method of measurement: DIP STICK.;The color of the urine. Timepoint: Before and After 1.2.3 days. Method of measurement: DIP STICK.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarshid Rahimi Bashar

Hamedan University of Medical Sciences

frahimi@umsha.ac.ir+98 81 3264 0025

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026