- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06090825
Cross-sectional Survey on Palliative Therapy for Pancreatic Cancer Patient
Real World Status of Palliative Care for Pancreatic Cancer Patients in China-a National Multi-center Cross-sectional Survey
Study Overview
Detailed Description
Pancreatic cancer is a highly malignant gastrointestinal tumor with only a 10% overall 5-year survival rate. More than 80% of patients are already in the advanced stage when diagnosed, losing the chance of surgery. Advanced pancreatic cancer progresses rapidly and chemoradiotherapy has limited efficacy, so palliative care is thought to play an important role in the treatment process. However, due to the late development of palliative care, there is a lack of data on real-world clinical palliative care for pancreatic cancer patients in China.
This study investigates the real-world current status of palliative care for pancreatic cancer patients by sending a web questionnaire to the doctors from the Department of General Surgery in more than 100 public tertiary teaching hospitals and about 350 public primary care units in the Chinese mainland. The survey aims to obtain the real status of palliative care and achieve a comprehensive understanding of how to develop palliative care in hospitals.
The questionnaire includes both subjective standards like the surgeons' opinion on the development of palliative therapy and objective standards such as dedicated beds and teams for palliative care.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Qiaofei Liu
- Phone Number: 8615201693370
- Email: qfliu@aliyun.com
Study Contact Backup
- Name: Yuze Hua
- Phone Number: 8617813719961
- Email: huayuze97@163.com
Study Locations
-
-
Beijing
-
Beijing, Beijing, China, 100730
- Recruiting
- Peking Union Medical College Hospital
-
Contact:
- Qiaofei Liu, MD
-
Principal Investigator:
- Qiaofei Liu, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Doctors from the General Surgery Department in Chinese public tertiary teaching hospitals and public primary care units
- Approval to participate
- Participants with a valid and complete questionnaire evaluated by 2 experienced surgeons
Exclusion Criteria:
- Refusal to participate
- Participants with an invalid or incomplete questionnaire
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Pancreatic cancer patients
|
Observational study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Descriptions and scores of real status of hospice care in different hospitals
Time Frame: 1 month
|
The primary outcome is objective standards and subjective scores of current status of palliative care to qutify the development of palliative care of different hospitals.
The score is evaluated by a follow-up questionnaire.
The maximum and minimum score is 10 and 0, respectively.
|
1 month
|
Collaborators and Investigators
Investigators
- Study Chair: Qiaofei Liu, Department of General Surgery, Peking Union Medical College Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- K4602
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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