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Trial · NCT07886541

Registered outcomes14

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

ListOutcomeTime frameDescription
PrimaryLength of hospital stayWithin the first 30 days after chest tube insertion.This is defined as the number of days from chest tube insertion to hospital discharge.
SecondaryDuration of chest tube drainage30 daysNumber of days between chest tube insertion and removal of chest tube
SecondaryDelayed discharge days30 days
The number of hospital days between completion of treatment and actual hospital discharge that are unrelated to the treatment of the parapneumonic pleural infection (e.g. awaiting nursing home placement, rehabilitation facility placement, home care arrangements, or other administrative or logistical delays).
SecondaryRe-intervention rates30 daysThe need for additional drainage procedures or surgery
SecondaryRe-admission rates30 daysNeed for re-admission
SecondaryMorbidity30 daysDefined as any deviation from the expected clinical course, including complications and (serious) adverse events
SecondaryMortality30-day and 1-year mortalityMortality (30-day and 1-year)
SecondaryType of antibiotic therapyUp to 3 months after initiation of antibiotic therapyType of antibiotic therapy
SecondaryDuration of antibiotic therapyUp to 3 months after initiation of antibiotic therapyDuration of antibiotic therapy (in days)
SecondaryType of analgesic use30 daysType of analgesic use
SecondaryDuration of analgesic use30 daysDuration of analgesic use (in days)
SecondaryHealthcare consumption costsThrough study completion (at 1, 3, 6, 9, and 12 months after randomization)
Healthcare consumption will be assessed using the iMTA Medical Consumption Questionnaire (iMCQ), an instrument designed to measure medical consumption, including contacts with healthcare providers, hospitalizations, medical procedures, medication use, and other healthcare services. The questionnaire will be used to assess healthcare consumption following randomization.
SecondaryProductivity loss costsThrough study completion (at 1, 3, 6, 9, and 12 months after randomization)
Productivity losses will be assessed using the iMTA Productivity Cost Questionnaire (iPCQ), a standardized instrument for measuring productivity losses for use in economic evaluations of healthcare. The questionnaire will be used to assess productivity losses following randomization.
SecondaryHealth-related quality of lifeThrough study completion (at baseline, 1 week, 2 weeks, 1, 3, 6, 9, and 12 months after randomization)
Health-related quality of life will be assessed using the EuroQol 5-Dimension 5-Level questionnaire (EQ-5D-5L). The questionnaire assesses five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has five response levels, ranging from no problems to extreme problems. Responses will be used to assess health-related quality of life.

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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