UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000017946
Receipt number R000020798
Scientific Title Intraoperative fluorescence staining of brain tumors using 5-aminolevulinic acid and purple-color light emitting diode
Date of disclosure of the study information 2015/06/17
Last modified on 2021/06/21 09:32:36

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Basic information

Public title

Intraoperative fluorescence staining of brain tumors using 5-aminolevulinic acid and purple-color light emitting diode

Acronym

Intraoperative fluorescence staining of brain tumors using 5-aminolevulinic acid

Scientific Title

Intraoperative fluorescence staining of brain tumors using 5-aminolevulinic acid and purple-color light emitting diode

Scientific Title:Acronym

Intraoperative fluorescence staining of brain tumors using 5-aminolevulinic acid

Region

Japan


Condition

Condition

Brain tumors

Classification by specialty

Neurosurgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate safety and efficacy of intraoperative fluorescence staining of brain tumors using 5-aminolevulinic acid (5-ALA) and purple-color light emiting diode

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Phase I,II


Assessment

Primary outcomes

Efficacy

Key secondary outcomes

Safety


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Medicine

Interventions/Control_1

Oral administration of 5-aminolevulinic acid

Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients undergoing surgical biopsy or resection for suspected malignant brain tumor based on preoperative imaging, including brain metastasis, malignant lymphoma, medulloblastoma, and germ cell tumor

Key exclusion criteria

Patients with suspected glioma: Alabel (5-aminolevulinic acid) is covered by insurance

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Nobuhito
Middle name
Last name Saito

Organization

The University of Tokyo Hospital

Division name

Department of Neurosurgery

Zip code

113-8655

Address

7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 Japan

TEL

03-5800-8853

Email

nsaito-tky@umin.net


Public contact

Name of contact person

1st name Shota
Middle name
Last name Tanaka

Organization

The University of Tokyo Hospital

Division name

Department of Neurosurgery

Zip code

113-8655

Address

7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655 Japan

TEL

03-5800-8853

Homepage URL

http://www.h.u-tokyo.ac.jp/neurosurg/rinsho/noushu.htm

Email

tanakas-tky@umin.ac.jp


Sponsor or person

Institute

The University of Tokyo
Faculty of Medicine
Department of Neurosurgery

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

None


Other related organizations

Co-sponsor

None

Name of secondary funder(s)

None


IRB Contact (For public release)

Organization

Office for Human Research Studies, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo

Address

7-3-1 Hongo, Bunkyo-ku, Tokyo

Tel

03-5841-0818

Email

ethics@m.u-tokyo.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

東京大学医学部附属病院(東京都)
The University of Tokyo Hospital (Tokyo, Japan)


Other administrative information

Date of disclosure of the study information

2015 Year 06 Month 17 Day


Related information

URL releasing protocol

N/A

Publication of results

Unpublished


Result

URL related to results and publications

N/A

Number of participants that the trial has enrolled

45

Results

Currently being analyzed

Results date posted

2021 Year 06 Month 21 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

Malignant brain tumors excluding gliomas

Participant flow

1. oral intake of 5-ALA before surgery
2. neurosurgery
3. tumor resection using fluorescence
4. light avoidance after surgery

Adverse events

None

Outcome measures

Currently being analyzed

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2010 Year 04 Month 26 Day

Date of IRB

2010 Year 04 Month 26 Day

Anticipated trial start date

2010 Year 04 Month 26 Day

Last follow-up date

2019 Year 08 Month 21 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 06 Month 17 Day

Last modified on

2021 Year 06 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020798


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name