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Search / Trial NCT05599217

Association Between Dietary Factors and Chronic Subdural Hematoma (DISH)

Launched by BEIJING TIANTAN HOSPITAL · Oct 25, 2022

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Chronic Subdural Hematoma Dietary Inflammatory Index Food Frequency Questionnaire Modified Frailty Index

ClinConnect Summary

The DISH trial is researching how different dietary habits and nutrition may be linked to chronic subdural hematoma (CSDH), a condition where blood collects on the surface of the brain. This study involves comparing the diets of patients who have CSDH with those who do not, to see if there are any significant differences. The trial is currently looking for participants who are between 18 and 90 years old, regardless of gender. To be eligible, patients in the CSDH group must have symptoms of the condition confirmed by brain scans, while healthy participants (the control group) should be matched in age and gender but do not have CSDH.

Participants can expect to share information about their diets and nutritional habits. Informed consent will be obtained from the participants or their family members, ensuring everyone understands the study before joining. It's important to note that certain individuals, such as those who have had previous brain surgery for other reasons or who have serious health issues, may not be eligible to participate. This trial aims to shed light on potential dietary factors that could influence the risk of developing CSDH, which may help in prevention and treatment strategies in the future.

Gender

ALL

Eligibility criteria

  • Case group (CSDH group)
  • Inclusion Criteria:
  • Patients (18 years to 90 years) presenting with clinical symptoms and neurological deficits of CSDH.
  • CSDH verified on cranial computed tomography or magnetic resonance imaging.
  • Written informed consent from patients or their next of kin according to the patient's cognitive status.
  • Control group (Healthy group)
  • Inclusion Criteria:
  • non-CSDH patients (18 years to 90 years) with matched age and gender.
  • Written informed consent from patients or their next of kin according to the patient's cognitive status.
  • Exclusion Criteria for both case and control group:
  • Previous intracranial surgery for any neurological disorders but chronic subdural hematoma before.
  • CSDH turned from acute subdural hematoma.
  • Existing malignant tumors, poor medication condition or severe comorbidity.
  • Difficulty in feeding requiring long-term enteral or parenteral nutrition support.
  • Dietary and nutritional survey is estimated to be completed difficultly.
  • Reproductive-age women without verified negative pregnancy testing.
  • Participating in other research.

About Beijing Tiantan Hospital

Beijing Tiantan Hospital, affiliated with Capital Medical University, is a leading medical institution in China renowned for its expertise in neurology, neurosurgery, and various other specialties. As a prominent clinical trial sponsor, the hospital is committed to advancing medical research and improving patient outcomes through innovative studies. With a focus on high-quality clinical trials, Beijing Tiantan Hospital adheres to rigorous ethical standards and regulatory requirements, fostering collaboration with academic institutions and industry partners to facilitate the development of cutting-edge therapies and interventions. Its state-of-the-art facilities and experienced research team enable the hospital to play a pivotal role in the global medical research landscape.

Locations

Zhengzhou, Henan, China

Beijing, , China

Yinchuan, Ningxia, China

Huangshan, Anhui, China

Lianyungang, Jiangsu, China

Patients applied

0 patients applied

Trial Officials

Weiming Liu, M.D.

Principal Investigator

Beijing Tiantan Hospital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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