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Trial · NCT02726620

Outcomes46

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPostoperative Acute Kidney InjuryWithin 7 days after surgeryPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARY30-day Mortality30 days after surgery
Per study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section). For a large group of patients no mortality information was available.
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIn-hospital MortalityAll postoperative days during a single hospital admission, expected median of 5 daysPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYPostoperative Acute Kidney Injury Stage 2Within 7 days after surgeryPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYPostoperative Rise in Creatinine LevelsWithin 7 days after surgery
Per study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section). Patients with no routine postoperative creatinine measurements are excluded from the analysis.
mg/dLMEDIAN
SECONDARYIncidence of a MAP < 60 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 55 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 50 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 60 mmHg for > 10 MinutesDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 55 mmHg for > 10 MinutesDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 50 mmHg for > 10 MinutesDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 60 mmHg for > 20 MinutesDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 55 mmHg for > 20 MinutesDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYIncidence of a MAP < 50 mmHg for > 20 MinutesDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYDepth and Duration of Intraoperative Hypotension - Threshold MAP 75 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).mmHg*minuteMEDIAN
SECONDARYDepth and Duration of Intraoperative Hypotension - Threshold MAP 70 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).mmHg*minuteMEDIAN
SECONDARYDepth and Duration of Intraoperative Hypotension - Threshold MAP 65 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).mmHg*minuteMEDIAN
SECONDARYDepth and Duration of Intraoperative Hypotension - Threshold MAP 60 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).mmHg*minuteMEDIAN
SECONDARYDepth and Duration of Intraoperative Hypotension - Threshold MAP 55 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).mmHg*minuteMEDIAN
SECONDARYDepth and Duration of Intraoperative Hypotension - Threshold MAP 50 mmHgDuring the anesthetic phase of the surgical procedure: an expected average of 2.5 hoursPer study protocol only patients with any MAP \< 65 mmHg will be included in the primary analysis (See also 'Participant Flow' section).mmHg*minuteMEDIAN

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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