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Safety and efficacy of diagnostic ultrasound combined with microbubble enhanced chemotherapy for pancreatic cancer

Safety and efficacy of diagnostic ultrasound combined with microbubble enhanced chemotherapy for pancreatic cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044721
Enrollment
Unknown
Registered
2021-03-26
Start date
2017-05-01
Completion date
Unknown
Last updated
2022-02-28

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

Conditions

pancreatic cancer

Interventions

experimental group:Ultrasound microbubble therapy for chemotherapy
control group:chemotherapy

Sponsors

Department of Ultrasound, Cancer Center of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The patients with locally advanced pancreatic cancer (stage III) with or without distant metastasis (stage IV); confirmed by histopathology or cytology were unresectable, regardless of the number of metastases; 2. Age 18-75 years old, male or female; 3. Oncological evaluation (ultrasound, CT or MRI) showed measurable and evaluable tumor lesions; 4. The estimated survival time was more than 3 months; 5. WBC >= 3.5x 10^9/L, ANC >= 1.5 x 10^9/L, PLT >= 80 x 10^9/L, Hb>= 90/L; 6. There was no significant abnormality in liver and kidney function: ALT and AST <= 2.5 times of the upper limit of normal value, urea and Cr <= 1,25 times of the upper limit of normal value, ALT and AST <= 5 times of the upper limit of normal value in patients with liver metastasis; 7. Cardiopulmonary function was basically normal; 8. There was no history of other malignant tumors; 9. Good compliance, no mental disorder.

Exclusion criteria

Exclusion criteria: 1. Pregnancy or lactation; 2. Allergic to chemotherapeutic drugs and hypersensitivity constitution; 3. Intestinal obstruction or incomplete intestinal obstruction; 4. There was a large amount of ascites; 5. With brain and bone metastasis; 6. Receiving other anti-tumor drugs or radiotherapy; 7. At the same time to participate in other clinical trials or chemotherapy end time is less than 4 weeks.

Design outcomes

Primary

MeasureTime frame
Cycle number of ultrasound treatment;Disease control rate;

Countries

China

Contacts

Public ContactZheng Liu

Department of ultrasound, Xinqiao Hospital, Chongqing

liuzhengs@163.com+86 13983406200

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026