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Trial · NCT06150898

Registered outcomes14

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

ListOutcomeTime frameDescription
PrimaryTo detect a reduced increase in systemic inflammation (from baseline to up to 24 hours after surgery) using peri-operative ketorolacUp to 24 hours after surgeryPlasma multiplex technology using cytometric bead arrays
PrimaryTo detect a reduced increase in systemic neurotransmitters (from baseline to up to 24 hours after surgery) using peri-operative pregabalinUp to 24 hours after surgeryLiquid Chromatography coupled to tandem Mass Spectrometry (LC-MS/MS)
PrimaryChange in biomarkers of metastasis at surgery from baselineAt surgeryTranscriptome profile and bioinformatic analysis
PrimaryChange in tumoral immune cells recruitment at surgery from baselineAt surgeryCharacterization of Tumour-infiltrating leukocyte subpopulations using RNA sequencing analysis from fresh frozen tissue sections
PrimaryChange in tumoral neurogenesis at surgery from baselineAt surgeryLevel of neurogenesis markers using RNA sequencing analysis from fresh frozen tissue section
PrimaryChange in tumoral neurotransmitters level at surgery from baselineAt surgeryUsing RNA sequencing analysis from fresh frozen tissue sections
PrimaryChange in Peripheral Blood Mononuclear Cells at surgery from baselineAt surgeryFluorescence activated cell sorting (FACS) analysis
PrimaryChange in systemic neuro-inflammatory mediators at surgery from baselineAt surgeryPlasma multiplex technology using cytometric bead arrays
PrimaryChange in systemic neurotransmitters at surgery from baselineAt surgeryPlasma multiplex technology using cytometric bead arrays
SecondaryChange in anxiety level at surgery from baselineAt surgery
Generalized Anxiety Disorder - 7 (GAD - 7) Anxiety score (natural number, range\[0 - 21\]. A score comprised between 0 - 4 indicates a minimal anxiety, 5-9 a mild anxiety, 10-14 a moderate anxiety and a 15-21 in a severe anxiety.
SecondaryPost-operative painUp to 48 hours after surgeryConsumption of morphine delivered by a programmable patient-controlled analgesia (PCA) infusion pump (number of requested and effectively delivered bolus/ 24h)
OtherBody Mass IndexThe day before surgeryCalculated: body mass (kg) divided by height squared (m²)
OtherBody compositionThe day before surgeryCalculated from multiple frequency bio-impedance measurements (in %, range \[0 - 100\])
OtherWaist-to-hip ratioThe day before surgeryWaist circumference (cm) divided by hip circumference (cm)

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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