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Perioperative glycemic control using artificial pancreas for surgical diabetes

Perioperative glycemic control using artificial pancreas for surgical diabetes - Perioperative glycemic control using artificial pancreas

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028036
Enrollment
160
Registered
2017-07-10
Start date
2017-07-10
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

Patients without diabetes mellitus who were received surgical operation including esophagectomy, gastrectomy, hepatectomy and pancreatectomy

Interventions

Perioperative glycemic control using artificial pancreas is performed to be targeting blood glucose ranging from 80 to 110 mg/dL during 2 days. Perioperative glycemic control using artificial pancreas

Sponsors

Kochi Medical School
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who undergo esophagectomy, gastrectomy, hepatectomy and pancreatectomy. 2. Patients without diabetes mellitus whose Hemoglobine A1c is 6.4% or below. 3. A performance status of 0-2 accord ing to the Eastern Cooperative Oncol ogy Group (ECOG) scale. 4. An age of 20 years and over. 5. Patients who are considered to survive for more than 3 months from the registration. 6. Vital organ functions are preserved within 14 days prior to entry. 7. Sufficient oral intake. 8. All patients gave written informed consent.

Exclusion criteria

Exclusion criteria: 1. Obvious infection or inflammation. 2. Serious cardiovascular diseases. 3. Serious concurrent disease such as intestinal palsy, small bowel obstraction, uncontrolable diabetes mellitus, renal failure, liver cirrhosis, and so on. 4. Massive ascites beyond the pelvic cavity or pleural effusion. 5. Women who are pregnant or hope to become pregnant during the study period. Men who wish their partner to become pregnant. 6. Patients judged inappropriate for the study by their physicians.

Design outcomes

Primary

MeasureTime frame
Serum IL-6 levels on on postoperative 3.

Secondary

MeasureTime frame
Morbidities including surgical Site Infection, mortality, hospitalization days, IL-6 at postoperative day 1, and CRP at postoperative day 3.

Countries

Japan

Contacts

Public ContactTsutomu Namikawa

Kochi Medical School Department of Surgery

tsutomun@kochi-u.ac.jp+81-88-880-2370

Outcome results

None listed

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