Optimization of blood examination from central venous ports in cancer patients.

Optimization of blood examination from central venous ports in cancer patients. - Optimization of blood examination from central venous ports in cancer patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000014794

Enrollment

Registered

2014-08-15

Start date

2014-08-18

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Patients with solid tumors

Interventions

blood collection from CV port blood collection from venipuncture

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Written informed consent 2) Decision of suitableness by principal investigator 3) Patients with chemotherapy for solid tumor 4) Patients enabling blood collection from venipuncture 5) Patients enabling blood collection from CV ports 6) Age >= 20 years 7) ECOG performance status of 0,1

Exclusion criteria

Exclusion criteria: 1) Decision of unsuitableness by principal investigator

Design outcomes

Primary

Measure	Time frame
to compare laboratory results of blood samples drawn from central venous port systems with the results from venipuncture	—

Secondary

Measure	Time frame
safety for blood collection from CV port	—

Countries

Japan

Contacts

Public ContactTakeshi Kotake

Kobe City Medical Center General Hospital medical oncology

t-kotake@kcho.jp078-302-4321

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026