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New drug combo may speed up hospital discharge after lung procedure

NCT ID NCT05643066

Symptom relief Sponsor: Fujian Provincial Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether adding a low dose of esketamine to the usual sedative propofol helps people recover and leave the hospital sooner after a bronchoscopy (a scope procedure to examine the lungs). The trial involved 246 adults scheduled for outpatient bronchoscopy. Researchers measured how many patients were ready to go home within 30 minutes after the procedure.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

246 people

The number who actually took part.

Started

Dec 2022

Finished

Dec 2023

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. American Society of Anesthesiologists (ASA) classification I-III; 2. Scheduled for ambulatory bronchoscopy. Exclusion Criteria: 1. Allergic or contraindications to studying drugs 2. History of obstructive sleep apnea-hypopnea syndrome 3. History of psychiatric illness 4. History of neurological disease 5. Pre-existing memory or cognitive impairment 6. History of seizure disorders 7. Pregnancy 8. Substance abuse or intake of drugs that affect the central nervous system 9. Inability to communicate in Mandarin Chinese. 10. Illiteracy

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Postoperative recovery

Contacts and locations

Locations

  • Fujian provincial hospital

    Fuzhou, Fujian, 350001, China

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