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Assessment of TauroLock™ in port catheter

A comparison of the effect of taurolidine and 4 % citrate(TauroLock™-HEP500) and Heparin use in Port catheter on the function of catheter and prevention of catheter complications in children with malignancy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201107049296N4
Enrollment
72
Registered
2023-10-22
Start date
2023-10-07
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Drugs used in chemotherapy. Chemotherapy session for neoplasm

Interventions

Intervention 1: Intervention group: All patients have a single-lumen Polysite(Vygon) catheter. Catheters are used for the purposes of chemotherapy and the transfer of blood and serum products and oth

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Months to 19 Years

Inclusion criteria

Inclusion criteria: Children who have recently been diagnosed with malignancy requiring chemotherapy Children who need Port-a-Cath for treatment of malignancy, not only transfusion. Consent of patients' parents and implicit consent of children with decision-making capacity Children Aged between 1 month to 19 years

Exclusion criteria

Exclusion criteria: Having congenital coagulation disorder Having non-tunneled Port-a-Cath History of congenital hematologic disorders

Design outcomes

Primary

MeasureTime frame
Serum Interleukin-6 level. Timepoint: Before intervention, 1 month after entering the study and 6 month after entring. Method of measurement: Patients' serologic examinations; the serum IL-6 level will be measured in pg/dl.;Duration of Port-a-Cath function. Timepoint: On the first medical contact and then every chemotherapy session or every month (whichever is earlier) up to 6 months. Method of measurement: The number of days that the port catheter has had a diagnostic or therapeutic function so that blood and fluids can move in both directions.

Secondary

MeasureTime frame
Serum CRP level. Timepoint: At the beginning of the study the 1 month later and 6 months later. Method of measurement: Serum CRP level will be measured by serologic examinations.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAziz Egbali

Iran University of Medical Sciences

eghbali.a@iums.ac.ir+98 21 2222 2041

Outcome results

None listed

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