UnknownNCT04834427

Safety and Efficacy Evaluation of S (+) - Ketamine in Children

This study has public registry information. It focuses on depression and currently lists study information in China.

Depression, Anxiety, ...DrugUp to 17 Years

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Study reference: NCT04834427. HopeStage can help you review the study, but cannot decide medical eligibility.

In plain English

Key information made simple

This study is comparing Conventional therapy + S (+)-Ketamine with Control group for people with depression or anxiety. Participants receive Conventional therapy + S (+)-Ketamine or Control group and complete study visits and assessments. Some participants may receive Control group instead of the study treatment, and direct benefit is not guaranteed.

What to expect

Your next step

The official record suggests in-person participation through a hospital, with sites including Chinese PLA General Hospital in Beijing. Participation appears to involve a study treatment together with follow-up visits and routine safety or progress checks. The main fit is usually being able to understand the study and consent and meeting the main study requirements, while common reasons not to take part include other factors that could make participation unsuitable. This is a later-stage study, which usually means the approach is being followed in broader real-world use.

Before joining

Questions to ask before joining

What are the exact eligibility criteria, and what could exclude someone?
How many visits, assessments, or follow-ups are expected, and over what period?
What risks, side effects, practical burdens, or alternatives should be understood first?
Who should be contacted to confirm locations, timing, compensation, and next steps?

Study clarity

Things to check before joining

Study start dateStarted: April 20, 2022

Time commitment: long follow-up or multiple visits
Study phase: Not available
Enrollment: Not available
Recruitment status: Unknown
Sponsor: Chinese PLA General Hospital
Sponsor type: Hospital / academic medical center
Main activity: medication or study treatment
Intervention: Not available
Source: Official registry link

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Public study data

Key study information

Official title: Safety and Efficacy Evaluation of S (+) - Ketamine in Children
Condition: Depression, Anxiety, ...
Study status: Unknown
Sponsor / lead affiliation: Chinese PLA General Hospital
Location / country: China
Registry: ClinicalTrials.gov
External trial ID: NCT04834427

Why this study may matter

This study may matter because it adds public evidence around depression. HopeStage presents it as a starting point for understanding the study, checking the official source, and preparing questions with a care team.

In practice

For you

Taking part may give access to a new approach being evaluated.

It requires regular visits and structured follow-up.

Requires travel, with in-person participation in China.

Official source

Registry reference

This page links back to the public source record so people can verify details directly with the registry and research team.

If you want the full study description, eligibility criteria, locations, and sponsor information in the original format, this is the place to check before taking the next step.

Official title: Safety and Efficacy Evaluation of S (+) - Ketamine in Children
Source: ClinicalTrials.gov
Official registry link: Open official registry
External trial ID: NCT04834427

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 Safety and Efficacy Evaluation of S (+) - Ketamine in Children?

This study is exploring medication or study treatment for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. It includes a comparison with a control group. Direct benefit is not guaranteed.

Who is behind this study, and what type of sponsor is it?

This study is sponsored by Chinese PLA General Hospital. Based on the sponsor name or official registry information, it appears to be a hospital or academic medical center. You should verify the details in the official registry record.

What does participation involve, what phase is it, and what should I ask about safety?

This study may involve medication or study treatment, study visits, and assessments. The time commitment is long follow-up or multiple visits. The study phase is not available in HopeStage data. Check the official source record to see whether a phase is listed. Enrollment is not available in HopeStage data. HopeStage cannot say whether a study is safe or right for you. Before joining, ask the research team about possible risks, time commitment, visits, side effects, compensation, safety monitoring, and whether participation may affect your current care.

Where can I verify the study details?

Use the official source record linked on this page to check the full study description, recruitment status, eligibility criteria, locations, sponsor information, phase, enrollment, contact details, and any listed risks or requirements.

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