UMIN-CTR Clinical Trial

Recruitment status Preinitiation
Unique ID issued by UMIN UMIN000026986
Receipt No. R000030940
Official scientific title of the study Phase 2 trial of utility and safety for bevacizumab in combination with adjuvant chemotherapy in cervical cancer
Date of disclosure of the study information 2017/05/01
Last modified on 2017/04/13 (Ver. 1)

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Basic information
Official scientific title of the study Phase 2 trial of utility and safety for bevacizumab in combination with adjuvant chemotherapy in cervical cancer
Title of the study (Brief title) Trial of adjuvant chemotherapy with bevacizumab in cervical cancer
Region
Japan

Condition
Condition Cervical cancer
Classification by specialty
Obsterics and gynecology
Classification by malignancy Malignancy
Genomic information NO

Objectives
Narrative objectives1 Safety and efficacy of bevacizumab combination with adjuvant chemotherapy
Basic objectives2 Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Disease-free survival
Key secondary outcomes Side effect

Base
Study type Interventional

Study design
Basic design Single arm
Randomization Non-randomized
Randomization unit
Blinding Open -no one is blinded
Control Self control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms 1
Purpose of intervention Treatment
Type of intervention
Medicine
Interventions/Control_1 paclitaxel(175mg/m2) + carboplatin(AUC5) + bevacizumab(15mg/kg) for 6 months
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
20 years-old <=
Age-upper limit
75 years-old >=
Gender Female
Key inclusion criteria 1)Diagnosis with cervical cancer.
2)PS 0 or 1
3)Consent from the patient.
4)Pathological examination recognized risk of recurrence.
Key exclusion criteria 1)Patients have severe fever.
2)Patients have a hystory acute myocardial infarction.
3)Patients have ileus symptom.
4)Patients have poor control of DM and HT and VTE.
Target sample size 50

Research contact person
Name of lead principal investigator Masahide Ohmichi
Organization Osaka medical college
Division name Obstetrics and gynecology
Address 2-7, Daigaku-machi, Takatuki-shi, Osaka, 569-8686, Japan
TEL 072-863-1221
Email gyn140@osaka-med.ac.jp

Public contact
Name of contact person Keisuke Ashihara
Organization Osaka medical college
Division name Obstetrics and gynecology
Address 2-7, Daigaku-machi, Takatuki-shi, Osaka, 569-8686, Japan
TEL 072-863-1221
Homepage URL
Email gyn140@osaka-med.ac.jp

Sponsor
Institute Osaka medical college
Institute
Department

Funding Source
Organization Osaka medical college
Organization
Division
Category of Funding Organization Other
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

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

Other administrative information
Date of disclosure of the study information
2017 Year 05 Month 01 Day

Progress
Recruitment status Preinitiation
Date of protocol fixation
2017 Year 04 Month 01 Day
Anticipated trial start date
2017 Year 04 Month 01 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Related information
URL releasing protocol
Publication of results Unpublished
URL releasing results
Results
Other related information

Management information
Registered date
2017 Year 04 Month 13 Day
Last modified on
2017 Year 04 Month 13 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000030940