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Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2 against local failure after chemoradiotherapy or radiotherapy for esophageal cancer

Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2 against local failure after chemoradiotherapy or radiotherapy for esophageal cancer - Photodynamic diagnosis (PDD) by using Talaporfin and Sie-P2

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000029734
Enrollment
10
Registered
2017-10-27
Start date
2018-04-07
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

esophageal cancer

Interventions

PDD

Sponsors

Nagoya City University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The patient of recurrent esopphageal cacner after CRT who will be trated by Photodynamic therapy(PDT) with Talaporfin. Local failure after CRT or RT:more than 50Gy 2.histologically proven local failure 3.either not candidates for salvage surgery or having a physical status that would make the surgery intolerable 4.lesions limited to within the muscularis propria 5.age more than 20 years old 6.the patient who has no disturbance in liver and kidney. 7.provision of written informed consent

Exclusion criteria

Exclusion criteria: 1. the patinet who can not be inserted endoscope 2. with malignant hypertension, conjestive heart failure, liver dysfunction, myocardil infarction within 3 months, endostage of liver cirrhosis, poor controled DM, severe lung fibrosis, active pneumonitis 3. with active infection 4. inability to comply the sun shade restrictions 5. porphyria 6. severe psychosomatic disturbance 7. allergy against Talaporfin 8. for women, pregnancy or lactation, or unwillingness to use contraception 9. T3 or T4 10. larger than 3cm in diameter 11. half the circumference of the lumen or less 12. invasion to the cervical esophagus 13. patients who judged by the investigator that enrollment was inappropriate

Design outcomes

Primary

MeasureTime frame
Safety and efficacy of PDD

Countries

Japan

Contacts

Public ContactHiromi Kataoka

Division of Gastroenterology Division of Gastroenterology

hkataoka@med.nagoya-cu.ac.jp052-851-5511

Outcome results

None listed

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