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The Clinical Research on the Relationship Between Depression and Gut Microbiota in TBI Patients

China50 participantsStarted 2016-08

Plain-language summary

Microbiome studies may be highlighted as crucial in the development of depression for TBI patients. The microbiota-gut-brain connection may further provide an opportunity for microbiota manipulation to treat the TBI patients with depression.This study is to investigate whether exist the relationship between depression and circadian rhythm of patients with TBI or not and focus the study on the potential of the host-microbiota interaction in regulating depression.

Who can participate

Age range

18 Years – 60 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. The mild TBI (mTBI) patients (a short loss of consciousness (\<30 min), and/or a short post-traumatic amnesia (PTA) (\< 24 h), a Glasgow Coma Scale (GCS) score between 13 and 15)
. clinical diagnosis of depression

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

the relationship between depression and circadian rhythm of patients with TBI

Timeframe: From three months to six months after traumatic brain injury

Trial details

NCT IDNCT02874027

SponsorGeneral Hospital of Ningxia Medical University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2017-05

Contact for this trial

Xia hechun, Bachelor

8613995109559 xhechun@aliyun.com

View on ClinicalTrials.gov More Traumatic Brain Injury With Brief Loss of Consciousness trials