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Where should you recover after surgery? a trial seeks the best path

NCT ID NCT07740772

Knowledge-focused Sponsor: Indonesia University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time

Summary

This study looks at adults recovering from elective surgery in two different care areas: the post-anesthesia care unit (PACU) and the high-care unit (HCU). The goal is to see which setting is linked to shorter hospital stays and fewer cases where patients need to be moved to intensive care. By tracking outcomes for about 386 patients, researchers hope to find the most effective way to manage postoperative recovery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If one care setting proves more effective, it could streamline postoperative recovery, shorten hospital stays, and reduce the need for intensive care.
What could go wrong
This is an observational comparison, so it cannot prove cause and effect. Results may vary by patient and hospital, and the findings may not apply to other settings.

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.

Participants

About 386 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2026

Expected to finish

Oct 2026

An estimate. End dates often move.

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.

Who is studied

Adult patients undergoing elective surgery at RSCM who receive postoperative observation in the PACU or HCU.

Ages

18 years and older

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: * Adult patients aged more than 18 years. * Patients undergoing elective surgery in the Kanigara RSCM, PESC, RPT, or Kirana operating rooms. * Patients undergoing postoperative observation in the PACU or HCU. * Patients classified as Level II or III based on the Modified Johns Hopkins Surgical Criteria. * Patients who are willing to participate in the study and sign the informed consent form. Exclusion Criteria: * Patients undergoing postoperative observation directly in the ICU. * Patients undergoing open-heart surgery. * Patients undergoing emergency surgery in the emergency operating room.

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Conditions

The condition(s) this trial relates to.

Postoperative Complications

As listed by the trial registrant

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

Complication postoperative Hospital length of stay Step up cases

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • RSUPN dr. Cipto Mangunkusumo

    RECRUITING

    Jakarta Pusat, Jakarta Special Capital Region, 10430, Indonesia

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