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Clinical research of low dose dopamine combined with conventional treatment in the treatment of moderately severe and severe acute pancreatitis

Clinical research of low dose dopamine combined with conventional treatment in the treatment of moderately severe and severe acute pancreatitis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035980
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Acute pancreatitis

Interventions

DA-1 group:DA 0.5 ug/(kg·min)
DA-2 group:DA 1 ug/(kg·min)
DA-3 group:DA 2 ug/(kg·min)
DA-stable:0.5-2 ug/(kg·min)
DA-lower level:0.5-2 µg/(kg·min)
control group:No intervention

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of acute pancreatitis: according to the 2012 Atlanta classification and definition revision international consensus, the diagnosis of acute pancreatitis needs 2 of the following three characteristics: (1) Abdominal pain is consistent with the characteristics of acute pancreatitis (persistent and severe upper abdominal pain often radiates to the back); (2) The activity of serum lipase (or amylase) was at least 3 times higher than the normal upper limit; (3) Enhanced CT or infrequent magnetic resonance imaging (MRI) or abdominal ultrasonography revealed characteristic changes in acute pancreatitis; 2. Patients admitted within 48 hours after the onset of the disease; 3. Aged 18 to 75 years old; 4. Patients who meet the diagnostic criteria of predicted severe acute pancreatitis (meet the diagnostic criteria of acute pancreatitis, and meet one of the following conditions in the acute phase): (1) PASS > 140; (2) CRP > 150 mg/L; 5. Patients or their family members (guardians) agree to participate in the study, sign informed consent, and agree to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients with hypertension level 2 or hypertension level 1 with poor control under drug treatment; 2. Patients with severe respiratory, cardiovascular, digestive and hematological diseases, as well as psychiatric and infectious diseases; 3. Patients with serious illness who need non medical treatment such as surgery and peritoneal lavage; 4. Patients with advanced tumor; 5. Patients with chronic renal failure caused by organic kidney disease; 6. Patients who were enrolled in other clinical trials 3 months before onset of disease; 7. Patients with pheochromocytoma; 8. Occlusive vascular diseases (or those with previous history), including arterial embolism, atherosclerosis, thromboangiitis obliterans, frostbite (such as frostbite), diabetic endarteritis and Raynaud's disease should be used with caution; 9. Patients with frequent ventricular arrhythmias; 10. Patients with poor circulation; 11. Women during pregnant stage and breast-feed stage.

Design outcomes

Primary

MeasureTime frame
heart rate;blood pressure;Dose limiting toxicity and maximum tolerable dose;pass;sap;

Secondary

MeasureTime frame
temperature;Respiratory rate;Main symptoms;laboratory characteristics;Local complications;systemic complications;hospital stay;ICU occupancy rate;SIRS;APACHE II;

Countries

China

Contacts

Public ContactCongying Chen

Shanghai First People's Hospital

cherrychencong@163.com+86 18116149147

Outcome results

None listed

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