Pancreatic Solid Lesions Clinical Trial
Official title:
The Comparison of Wet Suction Technique and Dry Suction Technique in Endoscopic Ultrasound-guided Fine-needle Aspiration (EUS-FNA) for the Outcomes in Pancreatic Solid Lesions: a Prospective, Randomized Controlled, Blinded Trial
Verified date | June 2021 |
Source | The Third Xiangya Hospital of Central South University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this randomized controlled trial is to evaluate whether wet suction technique (WST), compared with dry suction technique (DST), shall present a better outcome with regard to the diagnostic yield and specimen quality of patients with solid lesions in the pancreatics.
Status | Completed |
Enrollment | 50 |
Est. completion date | March 31, 2020 |
Est. primary completion date | September 30, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: 1. Age > 18 years, < 80 years 2. female or male 3. Patients are required to undergo EUS-FNA after undergoing imaging examination (MRI, CT, or ultrasonography) which identify that the pancreatic lesions are existing and solid. 4. Agree to attend this study and signed informed consent letter Exclusion Criteria: 1. bad physical condition, including hemoglobin = 8.0 g/dl, severe cardiorespiratory dysfunction, and so on 2. Coagulopathy (platelet count < 50,000/mm3, international normalized ratio > 1.5) or having taken oral anticoagulation agents such as aspirin or warfarin in the previous week 3. Be rejected by anesthesia 4. Acute pancreatitis in the previous 2 weeks 5. Pregnant or lactation period 6. Psychiatric disease, drug addiction, or other reason for unreliable follow-up or questionnaires 7. Don't agree to attend this study and absence of informed consent |
Country | Name | City | State |
---|---|---|---|
China | The third Xiangya Hospital of central south University | Changsha | Hunan |
Lead Sponsor | Collaborator |
---|---|
The Third Xiangya Hospital of Central South University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The primary outcome is defined as the overall diagnosis yield of solid lesions by EUS-FNA with each aspiration technique. | The primary outcome is defined as the overall diagnosis yield of solid lesions by EUS-FNA with each aspiration technique. | 20 weeks | |
Secondary | The second outcome is defined as the diagnose yield of first pass of solid lesions by EUS-FNA with each aspiration technique. | The second outcome is defined as the diagnose yield of first pass of solid lesions by EUS-FNA with each aspiration technique. | 20 weeks | |
Secondary | The third outcome is the diagnose yield in benign solid lesions by EUS-FNA with each aspiration technique. | The third outcome is the diagnose yield in benign solid lesions by EUS-FNA with each aspiration technique. | 20 weeks | |
Secondary | The forth outcome is the diagnose yield in malignant solid lesions by EUS-FNA with each aspiration technique. | The forth outcome is the diagnose yield in malignant solid lesions by EUS-FNA with each aspiration technique. | 20 weeks | |
Secondary | The fifth outcome is the diagnose yield in solid lesions in different parts of the pancreas by EUS-FNA with each aspiration technique. | The fifth outcome is the diagnose yield in solid lesions in different parts of the pancreas by EUS-FNA with each aspiration technique. | 20 weeks |
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