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Clinical research of diagnostic ultrasound combined with microbubble in increasing sensitivity of pancreatic cancer to chemotherapeutic drugs

Clinical research of diagnostic ultrasound combined with microbubble in increasing sensitivity of pancreatic cancer to chemotherapeutic drugs

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004557
Enrollment
Unknown
Registered
2014-04-21
Start date
2014-05-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Pancreatic Cancer

Interventions

test group:microbubble cavitation by local diagnostic ultrasound irritation

Sponsors

Department of Ultrasound, the Second Affiliated Hospital of Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Histologically or cytologically confirmed locally advanced pancreatic cancer patient; 2. Aged 18-75 years old, male or female; 3. Have a measurable tumor lesion for oncology assessment (ultrasound, CT or MRI); 4. Expected survival of three months or more, PS score 0-2; 5. WBC=3.5×10*9/L; ANC=1.5×10*9/L; PLT=80×10*9/L; Hb=90/L; 6. Normal liver and kidney function; ALT, AST = 2.5 times upper limit of normal; Urea, Cr = 1.25 times upper limit of normal; ALT, AST = 5 times upper limit of normal for patients with liver metastases; 7. Normal heart and lung function; 8. No history of other malignant tumors; 9. Good compliance, no mental disorder; 10. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Do not meet the inclusion criteria; 2. Pregnancy or breast-feeding; 3. Allergy or hypersensitive to chemotherapy drugs; 4. With obstruction or incomplete intestinal obstruction; 5. With massive ascites; 6. With brain or bone metastasis; 7. Receiving other anti-cancer drugs or radiation therapy; 8. Participating in other clinical trials or end time is less than four weeks of chemotherapy.

Design outcomes

Primary

MeasureTime frame
Objective response rate;Progress free survival;Time to symptom progress;

Secondary

MeasureTime frame
Overall survival;

Contacts

Public ContactLiu Zheng

Department of ultrasound, Xinqiao Hospital,

liuzhengs@163.com+86 13983406200

Outcome results

None listed

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