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Trial · NCT07889934

Enhanced Recovery After Surgery in Patients Undergoing Colorectal Cancer Surgery

NCT07889934, Not applicable, Completed, University of West Attica

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Enhanced Recovery After Surgery in Patients Undergoing Colorectal Cancer Surgery. Trials, record NCT07889934. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07889934

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Enhanced Recovery After Surgery in Patients Undergoing Colorectal Cancer Surgery
NCT number
NCT07889934
Status
Completed
Phases
Not applicable
Enrollment
91 participants, actual
Lead sponsor
University of West Attica
Conditions
Colorectal Cancer
Interventions
Enhanced Recovery After Surgery (ERAS) Pathway, Conventional Perioperative Care
First posted
2026-10-22
Last updated
2026-11-02

Source ClinicalTrials.gov

Registered outcomes14

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPostoperative Length of Hospital StayFrom the date of surgery to hospital discharge, up to approximately 30 days
Number of calendar days from the date of surgery to the date of hospital discharge, obtained from the hospital medical record. A shorter postoperative hospital stay indicates earlier discharge after colorectal cancer surgery.
SecondaryTime to First Postoperative MobilizationFrom surgery until first mobilization, assessed during the first postoperative day and thereafter if needed
Time from completion of surgery to the patient's first mobilization out of bed. Recovery time was recorded using predefined postoperative time categories: 0-6, 6-12, 12-18, 18-24, and more than 24 hours.
SecondaryTime to Full Postoperative MobilizationFrom surgery until full mobilizationTime from surgery until the patient achieved full postoperative mobilization. Time was recorded in predefined categories of 0-6, 6-12, 12-18, 18-24, and more than 24 hours.
SecondaryTime to Return of Gastrointestinal MotilityFrom surgery until return of gastrointestinal motilityTime from surgery to documented return of gastrointestinal motility. Recovery time was recorded using predefined categories of 0-6, 6-12, 12-18, 18-24, and more than 24 hours.
SecondaryTime to Postoperative Oral FeedingFrom surgery until resumption of oral feedingTime from surgery to the first postoperative oral intake of fluids or solids, recorded using predefined categories of 0-6, 6-12, 12-18, 18-24, and more than 24 hours.
SecondaryPostoperative Pain Intensity0-2, 2-6, 6-12, and 12-24 hours after surgery; postoperative days 1, 2, and 3; and at hospital dischargePostoperative pain intensity assessed using an 11-point Numeric Rating Scale (NRS; 0 = no pain, 10 = worst imaginable pain). Pain was assessed repeatedly during the postoperative period.
SecondaryOccurrence of Postoperative Complications and Adverse EventsFrom surgery until hospital discharge
Occurrence of one or more predefined postoperative complications or adverse events, including nausea, vomiting, constipation, drowsiness, sedation, fever, local inflammation, bleeding, urinary tract infection, urinary retention, ileus, and reoperation. Events were recorded individually and as a composite binary outcome indicating the occurrence of any complication or adverse event.
SecondaryTime to Urinary Catheter RemovalFrom surgery until urinary catheter removalTime from surgery to removal of the urinary catheter, recorded using predefined categories of 0-6, 6-12, 12-18, 18-24, and more than 24 hours.
SecondaryTime to Surgical Drain RemovalFrom surgery until drain removalTime from surgery to removal of postoperative surgical drains, recorded using predefined categories of 0-6, 6-12, 12-18, 18-24, and more than 24 hours.
SecondaryTime to Discontinuation of Intravenous TherapyFrom surgery until discontinuation of intravenous therapyTime from surgery to discontinuation of postoperative intravenous therapy, recorded using predefined categories of 0-6, 6-12, 12-18, 18-24, and more than 24 hours.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07889934

GET https://conductscience.org/api/trials/v1/NCT07889934/registered