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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06277986
Other study ID # KY20212018-F-2
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2021
Est. completion date September 1, 2024

Study information

Verified date January 2024
Source Xijing Hospital
Contact Jipeng Li
Phone +86-029-84771533
Email jiangxunliang1992@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Gastric cancer is one of the most common malignancies, the morbidity and mortality of which are among the highest. In cancer patients, the incidence of cachexia is very high, and even 80% of patients will eventually develop into cachexia. However, once gastric cancer patients develop cachexia, patients are unlikely to obtain clinically significant benefits from conventional treatment. Therefore, it is important to find biomarkers for early detection of cachexia. The investigators carried out a plasma-derived exosomal microRNA(miRNA) study for early diagnosis of cachexia in gastric cancer, and the development of early diagnosis kits for gastric cancer cachexia.


Description:

Gastric cancer is one of the most common malignancies, the morbidity and mortality of which are among the highest. In gastric cancer patients, the incidence of cachexia is very high, and even 80% of patients will eventually develop into cachexia. However, once gastric cancer patients develop cachexia, patients are unlikely to obtain clinically significant benefits from conventional treatment. Therefore, it is important to find biomarkers for early detection of cachexia. The investigators carried out a plasma-derived exosomal microRNA(miRNA) study for early diagnosis of cachexia in gastric cancer, and the development of early diagnosis kits for gastric cancer cachexia.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date September 1, 2024
Est. primary completion date September 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patients with gastric cancer diagnosed by histopathology or cytopathology 2. Complete clinical and pathological data 3. No previous or current mental illness or disturbance of consciousness Exclusion Criteria: 1. With multiple tumors or other malignant diseases 2. Combined with other chronic wasting and metabolic diseases 3. Past patients with non-tumor cachexia 4. People with mental illness or unable to cooperate

Study Design


Related Conditions & MeSH terms


Intervention

Other:
cachexia
Cachexia mainly manifests as weight loss. 1)weight loss >5% over past 6 months. 2)BMI<20 and any degree of weight loss >2%. 3)Appendicular skeletal muscle index consistent with sarcopenia and any degree of weight loss >2%.

Locations

Country Name City State
China Fourth Military Medical University Xi'an Shaanxi

Sponsors (1)

Lead Sponsor Collaborator
Xijing Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary BMI Calculate BMI based on changes in body weight in the past six months six months
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