Skip to content

Clinical effect of faecal bacteria transplantation combined with hepatic arterial chemoembolization in advanced hepatocellular carcinoma

Clinical effect of faecal bacteria transplantation combined with hepatic arterial chemoembolization in advanced hepatocellular carcinoma

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034100
Enrollment
Unknown
Registered
2020-06-23
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-29

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

Conditions

hepatocellular carcinoma

Interventions

experimental group:Facal microbiota transplantation

Sponsors

Mianyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Confirmed by clinical examination for liver cancer, liver cancer and diseases in Barcelona centre (BCLC) staging standard display as late, does not apply to patients with surgical treatment, patients survival time is expected to more than 3 months (based on the tumor type, stage, estimated lifetime comprehensive judgment), signed informed consent, research hospital ethics committee approval.

Exclusion criteria

Exclusion criteria: (1) Pregnant or lactating women; Drug users; Suspected or confirmed history of alcohol/drug abuse; (2) Previous history of abdominal surgery; (3) Having a disease that may cause impairment of gastrointestinal function. Such as diabetes, thyroid diseases, intestinal obstruction, Inflammatory bowel disease (IBD), etc. (4) Take antibiotics, non-steroidal anti-inflammatory drugs, microecological agents, gastrointestinal motional drugs, acid-inhibiting drugs and other drugs that affect intestinal flora 2 weeks before treatment; (5) A history of Spontaneous bacterial peritonitis (SBP) combined with gastrointestinal bleeding or Spontaneous bacterial peritonitis two weeks ago; (6) Other serious diseases (including serious infections, serious heart, kidney, respiratory, blood, endocrine, neuropsychiatric diseases) or other types of tumors; (7) A history of use of immunosuppressive agents, or other severe Immunodeficiency diseases, such as Human Acquired Immunodeficiency Virus (HIV) infection, rheumatic diseases, etc.

Design outcomes

Primary

MeasureTime frame
Clinical symptoms;Liver function;

Secondary

MeasureTime frame
Fecal flora;Adverse events;

Countries

China

Contacts

Public ContactLi xiao an

Department of Gastroenterology, Mianyang Central Hospital

435445611@qq.com+86 13880868858

Outcome results

None listed

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