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Canceled by the investigator. A Clinical Study of Preoperative Combined Use of Ulinastatin and Somatostatin to Reduce Complications of Pancreaticoduodenectomy for Pancreatic Cancer

A Clinical Study of Preoperative Combined Use of Ulinastatin and Somatostatin to Reduce Complications of Pancreaticoduodenectomy for Pancreatic Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072391
Enrollment
Unknown
Registered
2023-06-12
Start date
2020-01-01
Completion date
Unknown
Last updated
2023-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pancreatic caner

Interventions

Combination therapy with somatostatin and ulinastatin:Preoperative Combined Use of Ulinastatin and Somatostatin
Control group:No somatostatin or ulinastatin was used before surgery

Sponsors

Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age range from 18 to 75 years old (including boundary values), both male and female. 2. Patients who underwent open pancreaticoduodenectomy in the Department of Hepatobiliary Surgery of Sichuan Provincial People's Hospital and were pathologically confirmed as pancreatic cancer after surgery. 3. ECOG physical status score 0 ~ 1. 4. Subject must sign and date written informed consent. 5. Subjects must be willing and able to comply with the scheduled treatment regimen, laboratory tests, follow-up, and other study requirements.

Exclusion criteria

Exclusion criteria: 1. Preoperative treatment of pancreatic cancer (e.g. interventional, targeted, immunotherapy, etc.). 2. Use ulinastatin or somatostatin alone or in combination for less than 3 days. 3. Patients with missing clinical data and other surgical methods. 4. Pregnant and lactating women. 5. Patients with prior or concurrent other malignant tumors. 6. Participated in other clinical studies within the past 1 month. 7. The investigator assessed the subject's inability or unwillingness to comply with study protocol requirements. 8. The subjects withdrew from the study for various reasons and could not participate in the study again

Design outcomes

Primary

MeasureTime frame
postoperative complications;

Secondary

MeasureTime frame
Intraoperative indicators;

Countries

China

Contacts

Public ContactXiaolun Huang

Sichuan Provincial People's Hospital

huangxiaolun@med.uestc.edu.cn+86 199 7984 2491

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026