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Recruiting NCT07740772

Effectiveness of PACU vs HCU Postoperative Care

Observational Hospital Length of Stay Step up Cases Complication Postoperative

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Hospital Length of Stay, Step up Cases, Complication Postoperative. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Indonesia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of the Effectiveness of Elective Postoperative Care in the PACU Versus HCU Based on Postoperative Length of Stay and Number of Step-Up Cases

Overview

To determine the effectiveness of postoperative hospital length of stay and the number of ICU or HCU step-up cases among elective postoperative patients observed in the PACU and HCU.

Primary outcome measures

  • number of ICU or HCU step-up cases [Time frame: from the day of surgery until the patient is discharged from the hospital or the patient dies up to 30 days]
  • postoperative hospital length of stay [Time frame: from the day of surgery until the patient is discharged from the hospital or the patient dies up to 30 days]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Indonesia · 1 center
  • RSUPN dr. Cipto Mangunkusumo — Jakarta Pusat

Identifiers

NCT: NCT07740772 · 26-02-0218

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗