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Study of Hyperthermic intraperitoneal chemotherapy(HIPEC) for peritoneal dissemination and appendiceal mucinous neoplasm

Study of Hyperthermic intraperitoneal chemotherapy(HIPEC) for peritoneal dissemination and appendiceal mucinous neoplasm - Study of Hyperthermic intraperitoneal chemotherapy(HIPEC) for peritoneal dissemination and appendiceal mucinous neoplasm

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000016360
Enrollment
10
Registered
2015-01-28
Start date
2014-06-20
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

peritoneal dissemination and appendiceal mucinous neoplasm

Interventions

Hyperthermic intraperitoneal chemotherapy

Sponsors

Mie university gastrointestinal and pediatric surgery
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ?Patients with peritoneal metastasis of gastric cancer,colon cancer, or appendicecal mucosal neoplasm ?Patients with positive peritoneal cytology ?Except for cases having distant metastasis such as liver and lung, and cases having non-healing factor such as unresectable lymph node metastasis except for peritoneal metastasis

Exclusion criteria

Exclusion criteria: ?Patients with heart disease(Arrhythmia requiring acute myocardial infarction within 6 months after the onset of ischemic heart disease, a medical treatment) ?Patients with a history of cerebrovascular disorder of cerebral infarction, cerebral hemorrhage, etc. ?Patients of systolic blood pressure less than 80mmHg or hypotension ?During pregnancy, Women suspected of being pregnant and Lactating woman ?Patients with dementia ?Patients with a history of shock during extracorporeal circulation therapy ?Patients taking stop angiotensin converting enzyme inhibitors, is difficult prior to extracorporeal circulation therapy ?Patients admitted unsuitable for the clinical study by research investigator

Design outcomes

Primary

MeasureTime frame
Surgical factor(Blood loss, operative time, blood transfusion) ,and Perioperative factor(Complications, hospital stay, readmission rate after surgery) perioperative factor

Countries

Japan

Contacts

Public ContactMasaki Ohi

Mie University Hospital Department of Innovative Surgery

mohi@clin.medic.mie-u.ac.jp059-232-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026