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The Clinical Efficacy of Gegen Qinlian Tang Combined with Bifidobacterium Triple Viable Capsules in the Prevention and Treatment of Radiation Enteritis

The Clinical Efficacy of Gegen Qinlian Tang Combined with Bifidobacterium Triple Viable Capsules in the Prevention and Treatment of Radiation Enteritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000085
Enrollment
Unknown
Registered
2025-01-13
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Abdominal and pelvic malignant tumors

Interventions

Control group:None
Intervention Group:On the basis of the Bifidobacterium triple viable capsule group oral administration of Gegen Qinlian Tang with additions and subtractions is used
Combination drug intervention group:On the basis of the Bifidobacterium triple viable capsule group oral administration of Gegen Qinlian Tang with additions and subtractions is used

Sponsors

Jiujiang First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age greater than 18 years and less than 80 years; (2) All patients have been diagnosed with malignant tumors through cytological or pathological examinations and are candidates for abdominal or pelvic radiotherapy according to the guidelines; (3) Conscious and thinking clearly with good communication skills; (4) Family members and patients have been informed and are willing to cooperate with the experiment and have signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with a history of severe intestinal diseases including ischemic bowel disease ulcerative colitis Crohn's disease etc.; (2) Those who have received antibiotic treatment within the past 2 years; (3) Patients with severe liver and kidney dysfunction. (4) Those with other major illnesses who cannot cooperate with the experiment or who withdraw midway; (5) Individuals unwilling to disclose medical records or with incomplete information.

Design outcomes

Primary

MeasureTime frame
Acute Radiation Injury Grading Criteria / RTOG/EORTC Grading;

Countries

China

Contacts

Public ContactLingzhi Zeng

Jiujiang First People's Hospital

dawn3399@sina.com13879233399

Outcome results

None listed

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