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Trial · NCT07889934

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.
OtherPostoperative Hemoglobinpostoperative day 1Postoperative hemoglobin concentration measured in g/dL. Postoperative values were evaluated in relation to the corresponding preoperative value.
OtherPostoperative Hematocritpostoperative day 1Postoperative hematocrit measured as percentage (%). Postoperative values were evaluated in relation to the corresponding preoperative value.
OtherPostoperative White Blood Cell Countpostoperative day 1Postoperative white blood cell count measured in ×10³/μL. Postoperative values were evaluated in relation to the corresponding preoperative value.
OtherPostoperative Blood Glucosepostoperative day 1Postoperative blood glucose concentration measured in mg/dL. Postoperative values were evaluated in relation to the corresponding preoperative value.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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