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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03189277
Other study ID # CH-PT-002
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 14, 2017
Last updated June 15, 2017
Start date June 2017
Est. completion date September 2017

Study information

Verified date June 2017
Source Chinese Academy of Medical Sciences
Contact Yuankai Shi, MD
Phone 86-10-87788293
Email syuankaipumc@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This cross-sectional study, utilizing two sets of questionaire designed for patients and physicians respectively, aims at the epidemiology, the clinical features, and the current status of evaluation and management of lung cancer related pain in 20 participating hospitals in Northern China.


Description:

Lung malignancies have become the most common cause of mortality among patients with cancer in China. A significant proportion of lung cancer patients suffer from cancer related pain, however few studies have reported the prevalence and clinical features of such pain, especially in China.

This study is a cross-sectional survey in 20 hospitals in Northern China. We designed two separate series of questions to be answered by patients and cancer management professionals. In the patient questionaire, we collect information on the prevalence, location, intensity, impact on life of lung cancer related pain. Questions on how doctors evaluate and manage the pain are included in both the patients' and physicians' surveys. In the doctors' questionaire, we also assess current situation of cancer pain educational programs attended in medical schools and post graduation through related questions.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 2000
Est. completion date September 2017
Est. primary completion date September 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. The patient questionaire

- All patients (outpatient and inpatient) diagnosed with lung cancer visiting the participating hospitals on the designated day of investigation

- Informed consent must be obtained from the participating patients

2. The physician questionaire

- All physicians who receive lung cancer patients (outpatient and inpatient) in the participating hospitals on the designated day of investigation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (20)

Lead Sponsor Collaborator
Chinese Academy of Medical Sciences 307 Hospital of PLA, 309th Hospital of Chinese People's Liberation Army, Beijing Cancer Hospital, Beijing Chao Yang Hospital, Beijing Chest Hospital, Chinese PLA General Hospital, Daxing Hospital Beijing, Hebei Medical University Fourth Hospital, Henan Cancer Hospital, Inner Mongolia People's Hospital, Peking Union Medical College Hospital, Peking University First Hospital, Peking University Third Hospital, Peking University Third Hospital Yanqing Hospital, Shanxi Province Cancer Hospital, The First Affiliated Hospital of Zhengzhou University, The Hospital of Shunyi District Beijing, Tianjin Medical University Cancer Institute and Hospital, Tianjin Medical University General Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of cancer-related pain in lung cancer patients in 20 hospitals in northern China the proportion of self-reported pain related to cancer affecting the enrolled lung cancer patients over the past 24 hours 24 hours
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