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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000002116

Enrollment

5600

Registered

2009-06-25

Start date

2009-07-01

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

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

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

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.

Exclusion criteria

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.

Design outcomes

Primary

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

Secondary

Measure	Time frame
To investigate the correlation between above mentioned factors.	—

Countries

Japan

Contacts

Public ContactKoji Nakada

The Jikei University School of Medicine Department of Surgery

nakada@jikei.ac.jp03-3433-1111

Outcome results