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Effects of Tiaoqi Xiaoji Formula on Quality of Life in Patients with Advanced Pancreatic Cancer: A Multicenter Randomized Controlled Trial

Effects of Tiaoqi Xiaoji Formula on Quality of Life in Patients with Advanced Pancreatic Cancer: A Multicenter Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001607
Enrollment
Unknown
Registered
2026-06-26
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Advanced Pancreatic Cancer

Interventions

Experimental Group:Tiaoqi Xiaoji formula combined with chemotherapy

Sponsors

Xiyuan Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 and 75 years, with no restriction on gender; (2) Histologically or cytologically confirmed pancreatic ductal adenocarcinoma that meets the diagnostic criteria for locally advanced and metastatic pancreatic cancer; (3) According to the Eastern Cooperative Oncology Group (ECOG) performance status criteria (Zubrod-ECOG-WHO, ZPS), patients with an ECOG score of 0-2; (4) Patients with an expected survival of at least 3 months; (5) Patients with at least 1 measurable or assessable lesion; (6) Patients who voluntarily agree to participate in this study, sign the informed consent form, and have good compliance.

Exclusion criteria

Exclusion criteria: (1) Patients with other active malignant tumors; (2) Patients with severe primary diseases of the heart, brain, liver (serum bilirubin = 1.5 times the upper limit of normal), kidneys (serum creatinine = 1.5 times the upper limit of normal), hematopoietic system, etc., as judged by the investigator to be unsuitable for enrollment; (3) Patients with active infections or other serious complications that may affect the safety or outcome assessment of the trial; (4) Pregnant or breastfeeding women, or women planning pregnancy within the next 3 months; (5) Patients with known allergies to the investigational drug or its excipients; (6) Patients currently participating in other interventional clinical trials; (7) Patients with severe mental disorders, cognitive impairments, or communication difficulties that prevent them from completing questionnaire assessments and follow-ups; (8)Patients deemed unsuitable for participation in this study by the investigator.

Design outcomes

Primary

MeasureTime frame
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire–Core 30 scores ;

Secondary

MeasureTime frame
European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire–Pancreatic Cancer Module 26 Score;M. D. Anderson Symptom Inventory–Gastrointestinal Cancer Module Score;Hospital Anxiety and Depression Scale score Score;Eastern Cooperative Oncology Group Performance Status Score;Body Mass Index;Disease control rate;Objective response rate;Serum carbohydrate antigen 19-9 level;Neutrophil-to-Lymphocyte Ratio;Platelet-to-Lymphocyte Ratio;

Countries

China

Contacts

Public ContactBo Pang

Xiyuan Hospital of China Academy of Chinese Medical Sciences

pangbotommy@126.com13810166354

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026