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Can a recovery checklist help appendix patients go home sooner?

NCT ID NCT07401407

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study observed 193 adults who had emergency laparoscopic appendix surgery for uncomplicated appendicitis. Researchers wanted to see how closely hospitals followed a specific recovery plan called RICA (an ERAS pathway) and whether early discharge within 24 hours was safe and feasible. They collected data on complications, hospital stay length, readmissions, and patient satisfaction, without changing any usual care.

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

193 people

The number who actually took part.

Started

Dec 2022

Finished

Feb 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Who is studied

Adults aged 18-75 years undergoing urgent laparoscopic appendectomy for uncomplicated acute appendicitis in participating hospitals. The study evaluates adherence to the RICA (ERAS Zaragoza 2022) pathway in routine clinical practice, early discharge feasibility (8, 12, and 24 hours after surgery), and safety outcomes (complications, readmissions, reinterventions, and mortality) up to 30 days after surgery. No experimental intervention is introduced.

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: * Age ≥ 18 and ≤ 75 years. * Immunocompetent patients. * ASA physical status I-III. * Preoperative diagnosis of uncomplicated acute appendicitis (based on clinical assessment, laboratory tests, and imaging such as ultrasound and/or CT according to availability). * Indication for urgent appendectomy for uncomplicated appendicitis. * Laparoscopic approach. * Expected operative time \< 90 minutes. * Cooperative patient able to understand and follow instructions. * Voluntary participation and written informed consent. * Adequate social/family support (availability of a responsible adult for transport home and support during the first postoperative days). * Travel time from home to hospital \< 1 hour and access to transportation. * Acceptable home environment for recovery (telephone access and basic habitability/hygiene). Exclusion Criteria: * ASA physical status IV. * Age \< 18 years or \> 75 years. * BMI \> 35 kg/m² with significant respiratory or cardiovascular complications. * Ischemic heart disease class IV or acute myocardial infarction within the last 6 months. * Congestive heart failure NYHA class III-IV. * Sleep apnea or severe COPD, or need for home oxygen therapy. * Poorly controlled diabetes mellitus. * Severe psychiatric disorders, drug addiction, or severe alcoholism. * History of major anesthesia-related complications or malignant hyperthermia. * Epilepsy. * Pregnancy. * Use of anticoagulants, MAO inhibitors, systemic corticosteroids, or immunosuppressive drugs. * Complicated appendicitis (gangrenous or perforated appendicitis, abscess, diffuse peritonitis). * Severe sepsis. * Primary open appendectomy or conversion to open surgery. * Positive SARS-CoV-2 PCR or symptoms compatible with COVID-19.

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Conditions

The condition(s) this trial relates to.

appendicitis Patient Satisfaction

As listed by the trial registrant

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

Contacts and locations

Locations

  • Hospital Galdakao-Usansolo

    Galdakao, Vizcaya, 48960, Spain

  • Hospital General Universitario de Elche

    Elche, Alicante, 03203, Spain

  • Hospital Universitari Parc Taulí

    Sabadell, Barcelona, 08208, Spain

  • Hospital Universitari d'Igualada

    Igualada, Barcelona, 08700, Spain

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