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A Study on the Dominant Population for Yin Yang Gong Ji pill in the treatment of colorectal cancer based on the theory of "Lv Gong Lv Bu, Yi Ping Wei Qi"

A Study on the Dominant Population for Yin Yang Gong Ji pill in the treatment of colorectal cancer based on the theory of "Lv Gong Lv Bu, Yi Ping Wei Qi"

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077794
Enrollment
Unknown
Registered
2023-11-20
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-11-27

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

Conditions

metastatic colorectal cancer

Interventions

intervention group:Oral administration twice a day, 5 capsules each time, treatment period: 30 days (taking 20 days and resting for 10 days), treatment period = 3 months is considered positive exposur

Sponsors

Chongqing University Three Gorges Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Age = 18 years old, regardless of gender; ? Pathological staging of metastatic colorectal cancer with no chance of radical surgery; ? KPS score = 60 points; ? Expected survival time = 3 months; ? Without strict center of gravity, abnormal lung, liver, and kidney functions; ? Non grade II and above diarrhea (CTCAE v4.03 grade); ? Having measurable lesions that meet the RECIST 1.1 standard; ? Volunteer to join this study and sign an informed consent form;

Exclusion criteria

Exclusion criteria: ? Merge with other malignant tumors; ? Concomitant severe heart, liver, and kidney diseases and complications; ? There are various factors that affect the absorption of oral drugs, such as difficulty swallowing or intestinal obstruction. Suffering from malabsorption syndrome or other diseases that affect gastrointestinal absorption, or suffering from active peptic ulcer; ? Any unstable situation that may endanger patient safety and research compliance; ? Subjects with poor compliance or inability to cooperate in completing the study were judged by the researcher; ? Other situations that the researchers believe are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
overall survival;

Secondary

MeasureTime frame
progression-free survival;

Countries

China

Contacts

Public ContactWang Lei

Chongqing University Three Gorges Hospital

dr.wang-cacms@foxmail.com+86 173 8470 0550

Outcome results

None listed

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