UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029460
Receipt number R000033659
Scientific Title Evaluation of swallowing function after reconstruction surgery for oral,orophayrngeal, and hypopharyngeal cancer using 320-Detector-Row Multislice CT.
Date of disclosure of the study information 2017/10/31
Last modified on 2021/01/26 08:06:25

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Basic information

Public title

Evaluation of swallowing function after reconstruction surgery for oral,orophayrngeal, and hypopharyngeal cancer using 320-Detector-Row Multislice CT.

Acronym

Evaluation of swallowing function after surgery for oral,orophayrngeal, and hypopharyngeal cancer using multislice CT.

Scientific Title

Evaluation of swallowing function after reconstruction surgery for oral,orophayrngeal, and hypopharyngeal cancer using 320-Detector-Row Multislice CT.

Scientific Title:Acronym

Evaluation of swallowing function after surgery for oral,orophayrngeal, and hypopharyngeal cancer using multislice CT.

Region

Japan


Condition

Condition

orophayrngeal cancer

Classification by specialty

Oto-rhino-laryngology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To clarify the swallowing movement of the patient who received reconstruction surgery for oropharyngeal cancer using multislice CT.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Others

Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Movement of pharyngeal wall and hyoid bone, larynx during swallow.

Key secondary outcomes

Pharyngeal constriction ratio, Bolus residual ratio, Oral-pharyngeal transit time, MTF score, %LE, Swallowing pressure of pharynx, AsR score,


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

Other

Interventions/Control_1

Administer multislice CT at frequent checkup, once per person

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


Not applicable

Gender

Male and Female

Key inclusion criteria

(1) squamous cell carcinoma in head and neck region
(2) primary site is oropharynx
(3) received reconstruction surgery for oropahryngeal cancer between April 1, 2000 and March 31, 2016 at Nagoya university hospital.
(4) not received Radiation therapy before or after surgery
(5) available for clinical records
(6) not received Radiation therapy for another head and neck cancer
(7) not received radiation therapy for other cancer
(8) not have simultaneous or metachronous head and neck cancer

Key exclusion criteria

(1) minority
(2) have systemic infection
(3) have simultaneous or metachronous head and neck cancer
(4) fever over 38 degree
(5) pregnant
(6) have mental disease, and can not decision making
(7) have heart disease that not cured or during treatment
(8) reject to using clinical records

Target sample size

15


Research contact person

Name of lead principal investigator

1st name takashi
Middle name
Last name maruo

Organization

Nagoya university

Division name

Otorhinolaryngology

Zip code

4668560

Address

Tsurumai tyou 65, shouwa ward, nagoya city, aichi prefecture, japan

TEL

052-744-2323

Email

yasushif@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name takashi
Middle name
Last name maruo

Organization

Nagoya university hospital

Division name

Otorhinolaryngology

Zip code

466-8560

Address

Tsurumai tyou 65, shouwa ward, nagoya city, aichi prefecture, japan

TEL

052-744-2323

Homepage URL


Email

tmaruo@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya university

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Nagoya university hospital

Address

Tsurumai tyou 65, shouwa ward, nagoya city, aichi prefecture, japan

Tel

052-744-2323

Email

tmaruo@med.nagoya-u.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



Other administrative information

Date of disclosure of the study information

2017 Year 10 Month 31 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Open public recruiting

Date of protocol fixation

2017 Year 07 Month 30 Day

Date of IRB

2017 Year 09 Month 16 Day

Anticipated trial start date

2017 Year 12 Month 01 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 10 Month 06 Day

Last modified on

2021 Year 01 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000033659


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name