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Evaluation of hysteroscopic photo dynamic diagnosis for the diseases in the uterine cavity.

Evaluation of the efficacy of hysteroscopic photodynamic diagnosis using 5-aminolevrinic acid for diseases in the uterine cavity.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031180123
Enrollment
30
Registered
2019-02-14
Start date
2019-06-25
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

diseases in the uterine cavity(ex: uterine myoma, endometrial polyp, uterine corpus cancer, endometr diseases in the uterine cavity, uterine myoma, endometrial polyp, endometrial cancer, endometrial hyperplasia

Interventions

Patients are given aminolevrin acid 20mg/kg about four hours before hysteroscopic operation once. They are performed hysteroscopic photodynamic diagnosis during operation.
D015907, D000284

Sponsors

Banno Kouji
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients who have diseases in uterine cavity. Patients who plan to undergo hysteroscopic operation for those diseases at the department of obstetrics and gynecology of Keio university hospital.

Exclusion criteria

Exclusion criteria: 1. under 20 years old 2. BMI>30 3. the medical history of endometrial entirely curettage in recent 14 day2. 4. the allergic history for the analog of the porphyrin. 5. porphyria 6. the medicine that is known for the cause of photosensitivity (ex. tetracycline antibacterial agent, medicine of sulfonamide, new quinolone antibacterial agent, hypericin and St.John's Wort. 7. the possibility of pregnant or blest feeding. 8. the diabetes mellitus and/or hyperlipidemia which is not controlled. 9. other endocrine diseases which are not controlled. 10. considered inadequate for this trial by the principal investigator.

Design outcomes

Primary

MeasureTime frame
diagnostic accuracy for the malignant disease.

Secondary

MeasureTime frame
relationship between pathological findings and strength of the fluorescence adverse events (based on CTCAE v4.0-JCOG)

Contacts

Public ContactKouji Banno

Keio University School of Medicine

kbanno@keio.jp+81-3-3353-1211

Outcome results

None listed

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