Skip to content

Clinical Observation and Cellular Immune Mechanism Study of Wuda Granules in Improving Intestinal Congestion Reperfusion Injury Caused by Hepatic Blood Flow Blockage.

Clinical Observation and Cellular Immune Mechanism Study of Wuda Granules in Improving Intestinal Congestion Reperfusion Injury Caused by Hepatic Blood Flow Blockage.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000489
Enrollment
Unknown
Registered
2025-03-07
Start date
2025-03-13
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Intestinal congestion reperfusion injury caused by hepatic blood flow occlusion during hepatobiliary surgery.

Interventions

Test group:Wuda Granules + Conventional Treatment (Implement conventional treatment protocols, including antibiotic therapy, fluid replacement support therapy, and postoperative rapid rehabilitation n
Control group:Conventional treatment

Sponsors

Guangdong Proal Hosvincipital of Chinese Medicine Zhuhai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Age between 18 and 70 years regardless of gender; 2) Cases scheduled for laparoscopic liver resection due to diagnoses such as hepatolithiasis or liver tumors; 3) Liver function classified as Child-Pugh A; 4) Intraoperative hepatic portal occlusion performed using the Pringle maneuver; 5) Preoperative electrogastrogram indicating normal gastrointestinal electrical activity; 6) Willingness to participate in the study and provision of signed informed consent.

Exclusion criteria

Exclusion criteria: 1) History of previous abdominal surgery; 2) Cases with combined dysfunction of major systemic or organ systems; 3) Patients with moderate to severe liver cirrhosis or moderate to severe portal hypertension; 4) History of gastrointestinal bleeding due to portal hypertension; 5) Family history of genetic diseases or cases with comorbid immune-related diseases; 6) Prior treatment with TACE PVE or radiotherapy before surgery; 7) Use of molecular targeted therapy chemotherapy or immunotherapy before surgery; 8) Cases unable to comply with taking the trial medication; 9) Contraindications to Wuda Granules such as spleen and stomach weakness pregnancy or allergies to drug components should be excluded; 10) Women who are breastfeeding.

Design outcomes

Primary

MeasureTime frame
Malondialdehyde;

Secondary

MeasureTime frame
Clinical Indicators (NRS Pain Score, Abdominal Distension Grade, Time to First Flatus, Time to Return of Normal Bowel Sounds);Laboratory Indicators (Complete Blood Count, Urinalysis, Liver and Kidney Function, Biochemical Indicators, Diamine Oxidase, IL-1ß, TNF-a);

Countries

China

Contacts

Public ContactQiu Chengjiang

Guangdong Proal Hosvincipital of Chinese Medicine Zhuhai

chinavp83@163.com13430347207

Outcome results

None listed

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