UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000002116
Receipt number R000002578
Scientific Title A study to observe correlation between resection and reconstruction procedures employed for gastric neoplasms and development of postgastrectomy syndrome
Date of disclosure of the study information 2009/06/25
Last modified on 2017/08/08 18:14:46

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

A study to observe correlation between resection and reconstruction procedures employed for gastric neoplasms and development of postgastrectomy syndrome

Acronym

A study to observe correlation between resection and reconstruction procedures employed for gastric neoplasms and development of postgastrectomy syndrome

Scientific Title

A study to observe correlation between resection and reconstruction procedures employed for gastric neoplasms and development of postgastrectomy syndrome

Scientific Title:Acronym

A study to observe correlation between resection and reconstruction procedures employed for gastric neoplasms and development of postgastrectomy syndrome

Region

Japan


Condition

Condition

Gastric cancer patients who underwent various types of gastrectomy
(GIST patients who underwent gastric wedge resection are also included)

Classification by specialty

Gastrointestinal surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To examine health related quality of life and degree of postgastrectomy syndrome among patients who underwent various types of gastrectomy and reconstruction procedures.

Basic objectives2

Others

Basic objectives -Others

To study usefulness and validity of a questionnaire, which has been developed by a nationwide study group to assess health related quality of life and degree of postgastrectomy syndrome among patients who underwent surgery for gastric neoplasms.

Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

To examine the degree of generic QOL (SF-8), symptom specific QOL (GSRS), other abdominal symptoms, ingested amount, weight loss and satisfaction.

Key secondary outcomes

To investigate the correlation between above mentioned factors.


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

Male and Female

Key inclusion criteria

The inclusion criteria are as follows:
(1) Gastric cancer patients with pathologically confirmed stage IA or IB disease or patients with a GIST who underwent gastric wedge resection.
(2) Patients who underwent gastrectomy for the first time.
(3) Patients who were not treated with chemotherapy.
(4) Patients without any recurrence or distant metastasis.
(5) Patients with an interval of one year or longer after gastrectomy.
(6) Physical status 0 or 1.
(7) Fully capable of understanding and responding to the questionnaire.
(8) Without any other disease or previous surgery which may influence the results of questionnaire more than gastrectomy.
(9) Without any organ failure or mental disease.
(10) Written informed consent with date and signature of the said person.

Key exclusion criteria

(1) Active dual malignancy.
(2) Patients who underwent concomitant resection of other organ(s) due to another disease (co-resection equivalent to cholecystectomy being the exceptions).
(3) Considered as unsuitable to participate in the study by a surgeon who is in charge.

Target sample size

5600


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Koji Nakada

Organization

The Jikei University School of Medicine

Division name

Department of Surgery

Zip code


Address

3-25-8, nishishimbashi, minato-ku, Tokyo, 105-8461 Japan

TEL

03-3433-1111

Email

nakada@jikei.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Koji Nakada

Organization

The Jikei University School of Medicine

Division name

Department of Surgery

Zip code


Address

3-25-8, nishishimbashi, minato-ku, Tokyo, 105-8461 Japan

TEL

03-3433-1111

Homepage URL


Email

nakada@jikei.ac.jp


Sponsor or person

Institute

Department of Surgery, The Jikei University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

The Jikei University School of Medicine

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)

Japanese Society for Gastro-surgical Pathophysiology


IRB Contact (For public release)

Organization


Address


Tel


Email



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

静岡県立静岡がんセンター(静岡県)、市立豊中病院(大阪府)、広島大学病院(広島県)、千葉県がんセンター(千葉県)、横浜市立市民病院(神奈川県)、愛知県がんセンター中央病院(愛知県)、東京慈恵会医科大学病院(東京都)、千葉大学病院(千葉県)、高知大学病院(高知県)、栃木県立がんセンター(栃木県)京都大学病院(京都府) 、県立広島病院(広島県)、埼玉県立がんセンター(埼玉県)、山形県立中央病院(山形県)、名古屋大学病院(愛知県)、大阪厚生年金病院(大阪府)、川崎医科大学病院(岡山県)、函館五稜郭病院(北海道)、横浜市立大学附属市民総合医療センター(神奈川県)、帝京大学病院(東京都)、新潟県立がんセンター新潟病院(新潟県)、東京女子医科大学病院(東京都)、がん研有明病院(東京都)、岩手医科大学病院(岩手県)、JA廣島総合病院(広島県)、東邦大学医療センター大橋病院(東京都)、岐阜市民病院(岐阜県)、大阪医科大学病院(大阪府)、福岡大学病院(福岡県)、神戸市立医療センター中央市民病院(兵庫県)、佐久市立国保浅間総合病院(長野県)、筑波大学病院(茨城県)、北野病院(大阪府)、札幌医科大学病院(北海道)、浜松医科大学病院(静岡県)、がん・感染症センター都立駒込病院(東京都)、原町赤十字病院(群馬県)、九州大学病院(福岡県)、鹿児島大学病院(鹿児島県)、金沢医科大学病院(石川県)、長崎医療センター(長崎県)、国際医療福祉大学三田病院(東京都)、久留米大学病院(福岡県)、大阪府済生会野江病院(大阪府)、京都医療センター(京都府)、大手前病院(大阪府)、東京女子医科大学東医療センター(東京都)、東京慈恵会医科大学柏病院(千葉県)、城山病院(大阪府)、大分大学病院(大分県)、東北大学病院(宮城県)、横須賀市立うわまち病院(神奈川県)


Other administrative information

Date of disclosure of the study information

2009 Year 06 Month 25 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results

1. Nakada K, et al. Characteristics and clinical relevance of postgastrectomy syndrome assessment scale (PGSAS)-45: newly developed integrated questionnaires for assessment of living status and quality of life in postgastrectomy patients.
Gastric Cancer. 2015 Jan;18(1):147-58.

2. Terashima M, et al. Postgastrectomy Syndrome Assessment Scale (PGSAS)-45 and Changes in Body Weight are Useful Tools for Evaluation of Reconstruction Methods Following Distal Gastrectomy. Ann Surg Oncol. 2014 Jun;21 Suppl 3:S370-8.

3. Namikawa T, et al. Factors that minimize postgastrectomy symptoms following pylorus-preserving gastrectomy: assessment using a newly developed scale (PGSAS-45). Gastric Cancer. 2015 Apr;18(2):397-406.

4. Takiguchi N, et al. Long-term quality-of-life comparison of total gastrectomy and proximal gastrectomy by Postgastrectomy Syndrome Assessment Scale (PGSAS-45): a nationwide multi-institutional study. Gastric Cancer. 2015 Apr;18(2):407-16.

5. Misawa K, et al. Evaluation of postgastrectomy symptoms after distal gastrectomy with Billroth-I reconstruction using the Postgastrectomy Syndrome Assessment Scale-45 (PGSAS-45). Gastric Cancer. 2015 Jul;18(3):675-81.

6. Inada T, et al. Evaluation of QOL After Proximal Gastrectomy Using a Newly Developed Assessment Scale (PGSAS-45). World J Surg. 2014 Dec;38(12):3152-62.

7. Kawahira H, et al. Optimal Roux-en-Y reconstruction after distal gastrectomy for early gastric cancer as assessed using the newly developed PGSAS-45 scale.
Surg Today. 2015 Oct;45(10):1307-16.

8. Fujita J, et al. Assessment of postoperative quality of life following pylorus-preserving gastrectomy and Billroth-I distal gastrectomy in gastric cancer patients: results of the nationwide postgastrectomy syndrome assessment study.
Gastric Cancer 2016 Jan; 19(1): 302-311.

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

Completed

Date of protocol fixation

2009 Year 04 Month 27 Day

Date of IRB


Anticipated trial start date

2009 Year 07 Month 01 Day

Last follow-up date

2010 Year 12 Month 01 Day

Date of closure to data entry

2011 Year 02 Month 01 Day

Date trial data considered complete

2011 Year 04 Month 01 Day

Date analysis concluded

2012 Year 02 Month 01 Day


Other

Other related information

To compare the degree of postgastrectomy syndrome and the health related quality of life among patients who underwent various types of gastrectomy and reconstruction procedures.


Management information

Registered date

2009 Year 06 Month 24 Day

Last modified on

2017 Year 08 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000002578