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NCT04696276Completed

Implementing Enhanced Recovery After Surgery (ERAS) Pathways In Major Gynecologic Oncology Operations In Greece

Source: ClinicalTrials.gov · Last updated 26 Mar 2025

Brief summary (registry, in English)

The Enhanced Recovery After Surgery (ERAS) program includes preoperative counseling, fasting avoidance, non-opioid analgesia, fluid balance, normothermia and early mobilization. ERAS pathways were developed to reduce hospital length of stay, reduce costs and decrease perioperative opioid requirements, and be beneficial for patients. We propose the hypothesis that the ERAS pathway could reduce the length of stay (LOS) in hospital for patients undergoing major gynecologic oncology surgery (MGOS). Patients were randomly allocated in two groups: An ERAS pathway group including preoperative counseling, early feeding/mobilization, and opioid-sparing multimodal analgesia; and a classic model group of post operative recovery as control.

Status (registry)
Completed
Study type
Interventional
Enrollment
101 (actual)
First submitted
8 Nov 2020
Start date
6 Jan 2020
Primary completion date
31 Dec 2023
Lead sponsor
University of West Attica
NCT number
NCT04696276

What you commit to

  • Study type: Interventional
  • Participants enrolled: 101
  • From 6 Jan 2020 to the primary completion date, 31 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients receiving treatment for chronic pain
  • Patients receiving antipsychotic therapy, Psychopathy

Other illness

  • They have acute or chronic kidney and / or liver disease
  • History or family history of malignant hyperthermia
  • Known allergy to propofol, desflurane, or any other anesthetic agent
  • Impairment of cognitive function or communication
  • History of postoperative delirium

Other

  • Refusal to sign consent

Who the study is looking for

  • Greek language speakers
  • Have complete mental clarity
  • Age \>18 years

Age in the registry: 18 years to 79 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Saint Savvas Anticancer Hospital
Coordinator of this site? Confirm its status
AthensGreeceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.