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NCT07816900Completed

Efficacy and Safety of Da-Cheng-Qi Decoction in Severe Acute Pancreatitis

Efficacy and Safety of Da-Cheng-Qi Decoction in the Acute Stage of Severe Acute Pancreatitis: a Single-Center, Prospective, Randomized, Controlled Trial

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

This single-center prospective randomized controlled trial evaluated Da-Cheng-Qi Decoction (DCQD) as the acute-stage intervention of an integrated traditional Chinese and Western medicine whole-stage treatment protocol for severe acute pancreatitis (SAP). Sixty adults with SAP and intra-abdominal hypertension (IAP ≥ 12 mmHg) were randomized within 72 h of onset to receive standard Western treatment plus DCQD (100 mL via nasogastric tube twice daily for 7 days) or standard Western treatment alone. The primary outcome was intra-abdominal pressure measured by standardized bladder manometry every 12 h for 7 days. Secondary outcomes included stool output, length of hospital and ICU stay, and 28-day mortality. The trial was conducted at the Emergency Intensive Care Unit of Ruijin Hospital between April 2026 and July 2026.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
8 Sept 2026
Start date
1 Apr 2026
Primary completion date
5 Jul 2026
Lead sponsor
Shanghai Jiao Tong University School of Medicine
NCT number
NCT07816900

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 1 Apr 2026 to the primary completion date, 5 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Urinary tract infection or prior bladder surgery (precluding bladder manometry)

Other illness

  • Advanced malignancy (pancreatic, hepatobiliary, or gastrointestinal)
  • Severe chronic organ failure
  • Autoimmune disease or immunosuppression
  • Intra-abdominal hemorrhage
  • Allergic constitution or known allergy to study medication
  • Psychiatric illness

Age

  • Age \<18 or \>80 years

Other

  • Pregnancy or lactation

Who the study is looking for

  • Severe acute pancreatitis diagnosed according to the revised Atlanta classification
  • Age 18-80 years
  • Disease onset within 72 h
  • Intra-abdominal hypertension (IAP \>= 12 mmHg) within 24 h of admission
  • Written informed consent obtained

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emergency Department, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.