Dachaihu Decoction Compound and Rhubarb Single Medicine in the Treatment of Acute Pancreatitis
Primary Purpose
Acute Pancreatitis
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Dachaihu decoction compound
Rhubarb single medicine
Regular therapies
Sponsored by
About this trial
This is an interventional treatment trial for Acute Pancreatitis focused on measuring Acute Pancreatitis, Dachaihu Decoction Compound, Rhubarb Single Medicine
Eligibility Criteria
Inclusion Criteria:
- Age from 18 to 65 years old
- Meet the diagnostic criteria of western medicine for acute pancreatitis, within 48 hours of onset
- Consent of the subjects, who sign the informed consent form
Exclusion Criteria:
- Women who are pregnant or breastfeeding
- Acute abdomen such as organic intestinal obstruction, gastrointestinal perforation, purulent cholangitis, etc.
- Patients with a history of severe heart, liver, kidney and other important organ diseases
- Patients with mental illness and malignant tumors
- People who have allergies, or are allergic to a certain drug ingredient
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Other
Arm Label
DDC(Dachaihu decoction compound) Group
RSM(rhubarb single medicine) Group
N Group
Arm Description
Treated with Dachaihu decoction compound and regular therapies
Treated with rhubarb single medicine and regular therapies
Treated with regular therapies and without traditional Chinese medicine
Outcomes
Primary Outcome Measures
Significant and effective rate
Significant and effective rate after 7 days of treatment
Secondary Outcome Measures
Full Information
NCT ID
NCT04990336
First Posted
July 27, 2021
Last Updated
March 22, 2022
Sponsor
Fifth Affiliated Hospital, Sun Yat-Sen University
1. Study Identification
Unique Protocol Identification Number
NCT04990336
Brief Title
Dachaihu Decoction Compound and Rhubarb Single Medicine in the Treatment of Acute Pancreatitis
Official Title
Comparison of Clinical Efficacy of Dachaihu Decoction Compound and Rhubarb Single Medicine in the Treatment of Acute Pancreatitis
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
January 31, 2029 (Anticipated)
Study Completion Date
July 31, 2029 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fifth Affiliated Hospital, Sun Yat-Sen University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A large number of clinical studies have shown that oral administration, external application or enema of Chinese medicine can promote the recovery of gastrointestinal function and the absorption of pancreatic inflammation. The aims of the study is to explore the application of Dachaihu Decoction Compound (DDC)and Rhubarb Single Medicine (RSM) in the Treatment of Acute Pancreatitis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Pancreatitis
Keywords
Acute Pancreatitis, Dachaihu Decoction Compound, Rhubarb Single Medicine
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
306 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
DDC(Dachaihu decoction compound) Group
Arm Type
Experimental
Arm Description
Treated with Dachaihu decoction compound and regular therapies
Arm Title
RSM(rhubarb single medicine) Group
Arm Type
Active Comparator
Arm Description
Treated with rhubarb single medicine and regular therapies
Arm Title
N Group
Arm Type
Other
Arm Description
Treated with regular therapies and without traditional Chinese medicine
Intervention Type
Combination Product
Intervention Name(s)
Dachaihu decoction compound
Intervention Description
Dachaihu decoction compound includes Bupleurum, Rhubarb, Citrus aurantium, Scutellaria, Pinellia, White Peony, Jujube, Ginger.
Intervention Type
Drug
Intervention Name(s)
Rhubarb single medicine
Intervention Description
Rhubarb single medicine
Intervention Type
Combination Product
Intervention Name(s)
Regular therapies
Intervention Description
Regular therapies, such as fluid therapy, for acute pancreatitis
Primary Outcome Measure Information:
Title
Significant and effective rate
Description
Significant and effective rate after 7 days of treatment
Time Frame
7 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age from 18 to 65 years old
Meet the diagnostic criteria of western medicine for acute pancreatitis, within 48 hours of onset
Consent of the subjects, who sign the informed consent form
Exclusion Criteria:
Women who are pregnant or breastfeeding
Acute abdomen such as organic intestinal obstruction, gastrointestinal perforation, purulent cholangitis, etc.
Patients with a history of severe heart, liver, kidney and other important organ diseases
Patients with mental illness and malignant tumors
People who have allergies, or are allergic to a certain drug ingredient
12. IPD Sharing Statement
Learn more about this trial
Dachaihu Decoction Compound and Rhubarb Single Medicine in the Treatment of Acute Pancreatitis
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