Back to all studies
CompletedNCT05917379

The Efficacy and Safty of FMT in people with CID

This study is completed. It focuses on anxiety and currently lists study information in China.

Anxiety, Depression, ...BiologicalFrom 18 Years to 60 Years

The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

Then choose your country and confirm availability with each study site.

In plain English

Key information made simple

What is this study testing?

This study is testing whether fecal microbiota may be useful for adults experiencing anxiety.

What would participation involve?

Participants may complete study activities around fecal microbiota, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in China.

Who is it mainly for?

This study appears to be mainly for adults with anxiety.

What should you check before joining?

Ask about whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.

Your next step

Check the study details

Check the official source, then confirm these points with the research team.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    Where are visits, can any be remote, and how much time is needed?

  • Costs and support

    What costs, reimbursement or compensation apply?

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateStarted: October 8, 2023
Recruitment status
Completed
Enrollment listed in the registry
80
Sponsor
Peking University Sixth Hospital
Sponsor type
University
Study type
Biological
Intervention type
BIOLOGICAL, DIETARY_SUPPLEMENT, OTHER
Study phase
Phase 1, Phase 2This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
Locations
China
Age range
From 18 Years to 60 Years
Official registry ID
NCT05917379
Official title
The Safety and Efficacy of Fecal Microbiota Transplantation in Patients With Chronic Insomnia Disorder

Ask HopeStage to help me review this study

This record does not confirm open recruitment. We can help you understand it and explore other studies.

Loading the security check...
Study ID: NCT05917379. We help you review the study, but cannot decide medical eligibility.

Check recruitment and locations

Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.

View official study record (opens in a new tab)

The overall study status can differ from each site's status. Open a country to see its locations and their registry status.

China · 7 sites
  • Hefei Fourth People's Hospital/Anhui Mental Health Center
    Hefei, Anhui
    Site status: Not listed — confirm with the team
  • Department of Psychiatry, The Second Affiliated Hospital of Anhui Medical University
    Hefei, Anhui
    Site status: Not listed — confirm with the team
  • Peking University Six Hospital
    Beijing, Beijing Municipality
    Site status: Not listed — confirm with the team
  • Department of Psychiatry, The First Affiliated Hospital of Chongqing Medical University
    Chongqing, Chongqing Municipality
    Site status: Not listed — confirm with the team
  • Department of Physical Therapy, The Second Affiliated Hospital of Xinxiang Medical University
    Xinxiang, Henan
    Site status: Not listed — confirm with the team
  • Institute of Brain Science and Brain-inspired Research, Shandong First Medical University and Shandong Academy of Medical Sciences
    Jinan, Shandong
    Site status: Not listed — confirm with the team
  • Department of Psychiatry, First Hospital of Shanxi Medical University
    Taiyuan, Shanxi
    Site status: Not listed — confirm with the team
In practice

For you

Participation may contribute to research. Personal benefit is not guaranteed.

Ask the research team to explain the activities, time commitment, and follow-up involved.

Study sites are listed. Confirm the relevant site and any travel before making plans.

Important

Not medical advice

Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com

FAQ

Questions about this study

What is this study trying to understand?

This study is exploring observational follow-up for people with anxiety. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.

Does this study involve biological samples, imaging, or biomarkers?

This appears to be a biological / biomarker / imaging study involving fecal microbiota, Placebo, synbiotics. Phase 1 studies usually focus mainly on safety, tolerability, dosage, and side effects. They often involve healthy volunteers, but not always. Some Phase 1 studies include people living with the target condition.

Who might this study be for?

This study may concern people with anxiety; age range: From 18 Years to 60 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.

What would I likely need to do?

You may need to provide biological samples, complete lab tests, or take part in imaging or measurement procedures. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.

What should I check about samples, imaging, data, and possible discomfort?

If the study involves samples, imaging, or biomarkers, ask what is collected, how it is stored, who can access results, whether there may be discomfort, and whether results are shared with you. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.

Will I need to travel or attend in-person visits?

The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.

Who is behind this study?

This study is sponsored by Peking University Sixth Hospital, which appears to be a university. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.

Can I still join this study?

The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.

Explore other studies

Want to find a study that may fit you better?

Answer a few simple questions to explore HopeStage studies by condition, country, and situation.

Find a study that may fit me