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CompletedNCT07193901

Safety study of Efficacy, Safety, and Pharmacokinetic Characteristics of (R)-Ketamine Hydrochloride Nasal Spray in depression

This study is completed in China. It is testing Efficacy, Safety, and Pharmacokinetic Characteristics of (R)-Ketamine Hydrochloride Nasal Spray for depression.

Depression, SuicidalityDrugFrom 18 Years to 64 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 Low Dose PRT042 nasal spray may be useful for adults experiencing depression.

What would participation involve?

Participants may receive Low Dose PRT042 nasal spray, 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 depression.

What should you check before joining?

Ask about the dose, safety monitoring, and possible side effects, 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: May 27, 2025
Recruitment status
Completed
Enrollment listed in the registry
98
Sponsor
Sichuan Purity Pharmaceutical Technology Co., Ltd.
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
China
Age range
From 18 Years to 64 Years
Official registry ID
NCT07193901
Official title
A Randomized, Double-blind, Placebo-controlled Phase Il Study to Evaluate the Efficacy, Safety, and Pharmacokinetic Characteristics of (R)-Ketamine Hydrochloride Nasal Spray in Patients With Depression and Acute Suicidal Ideation or Behavior

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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 · 15 sites
  • The Sixth Hospital of Peking University
    Beijin
    Site status: Not listed — confirm with the team
  • BEIjing AnDing hospital capital medical university
    Beijing
    Site status: Not listed — confirm with the team
  • Beijing Huilongguan Hospital
    Beijing
    Site status: Not listed — confirm with the team
  • Brain Hospital of Hunan Province
    Changsha
    Site status: Not listed — confirm with the team
  • The Second Xiangya Hospital of Central South University
    Changsha
    Site status: Not listed — confirm with the team
  • The Fourth People's Hospital of Chengdu
    Chengdu
    Site status: Not listed — confirm with the team
  • Hangzhou Seventh People's Hospital
    Hangzhou
    Site status: Not listed — confirm with the team
  • Hefei Fourth People's Hospital(Anhui Mental Health Prevention and Treatment Center)
    Hefei
    Site status: Not listed — confirm with the team
  • The fourth affiliated hospital of Anhui medical university
    Hefei
    Site status: Not listed — confirm with the team
  • The Affiliated Hospital of Southwest Medical University
    Luzhou
    Site status: Not listed — confirm with the team
  • The First Affiliated Hospital of Nanchang University
    Nanchang
    Site status: Not listed — confirm with the team
  • The affiliated Kangning Hospital of Ningbo University
    Ningbo
    Site status: Not listed — confirm with the team
  • Suzhou Guangji Hospital
    Suzhou
    Site status: Not listed — confirm with the team
  • Wuxi Mental Health Center
    Wuxi
    Site status: Not listed — confirm with the team
  • Zhumadian Second People's Hospital(Zhumadian Psychiatric Hospital )
    Zhumadian
    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 medication or study treatment for people with depression. 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 a medication?

This appears to be a medication / drug study involving Low Dose PRT042 nasal spray, median Dose PRT042 nasal spray, high dose PRT042 nasal spray, placebo. Phase 2 studies usually explore whether the intervention may work, while continuing to monitor safety.

Who might this study be for?

This study may concern people with depression; age range: From 18 Years to 64 Years. The criteria appear fairly specific, 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 take a study treatment and have regular medical follow-up. 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 side effects, interactions, or treatment changes should I check?

If the study involves a medication, ask whether it is already approved, experimental, or being tested for a new use. Check possible side effects, interactions with current treatment, dose changes, monitoring, and what happens if you feel worse. 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 Sichuan Purity Pharmaceutical Technology Co., Ltd., which appears to be a pharmaceutical company. 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.

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