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Trial · NCT01549652

Outcomes12

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Objective Opioid Withdrawal Score (OOWS) From Baseline (Prevention of Opioid Withdrawal)Baseline; 15 minutes following last naloxone doseParticipants in the Prevention of Opioid Withdrawal Arm were analyzed.units on a scaleMEAN
SECONDARYChange in Subjective Opioid Withdrawal Score (SOWS) From Baseline (Prevention of Opioid Withdrawal)Baseline; 15 minutes following last naloxone doseParticipants in the Prevention of Opioid Withdrawal Arm were analyzed.units on a scaleMEAN
SECONDARYBeck Depression Inventory Score (BDIS) Change From Baseline (Prevention of Opioid Withdrawal)2 study days 1 month apart (at the start of each study visit)Participants in the Prevention of Opioid Withdrawal Arm were analyzed.units on a scaleMEAN
SECONDARYProfile of Mood States (POMS) Change in Score From Baseline (Prevention of Opioid Withdrawal)Baseline; 15 minutes following last naloxone doseParticipants in the Prevention of Opioid Withdrawal Arm were analyzed.units on a scaleMEAN
SECONDARYChange in Pain Visual Analog Scale (VAS) From Baseline (Prevention of Opioid Withdrawal)2 study days 1 month apart (at the start of each study visit)Participants in the Prevention of Opioid Withdrawal Arm were analyzed.units on a scaleMEAN
SECONDARYChange in Roland-Morris Disability Index (RMDI) From Baseline (Prevention of Opioid Withdrawal)2 study days 1 month apart (at the start of each study visit)Participants in the Prevention of Opioid Withdrawal Arm were analyzed.units on a scaleMEAN
PRIMARYChange in Objective Opioid Withdrawal Score From Baseline (Prevention of Physical Dependence)Baseline; 15 minutes following last naloxone doseParticipants in the Prevention of Physical Dependence Arm were analyzed.units on a scaleMEAN
SECONDARYChange in Subjective Opioid Withdrawal Score From Baseline (Prevention of Physical Dependence)Baseline; 15 minutes following last naloxone doseParticipants in the Prevention of Physical Dependence Arm were analyzed.units on a scaleMEAN
SECONDARYBeck Depression Inventory Score (BDIS) Change From Baseline (Prevention of Physical Dependence)2 study days 1 month apart (at the start of each study visit)Participants in the Prevention of Physical Dependence Arm were analyzed.units on a scaleMEAN
SECONDARYProfile of Mood States (POMS) Change in Score From Baseline (Prevention of Physical Dependence)Baseline; 15 minutes following last naloxone doseParticipants in the Prevention of Physical Dependence Arm were analyzed.units on a scaleMEAN
SECONDARYChange in Pain Visual Analog Scale (VAS) From Baseline (Prevention of Physical Dependence)2 study days 1 month apart (at the start of each study visit)Participants in the Prevention of Physical Dependence Arm were analyzed.units on a scaleMEAN
SECONDARYChange in Roland-Morris Disability (RMDI) Index From Baseline (Prevention of Physical Dependence)2 study days 1 month apart (at the start of each study visit)Participants in the Prevention of Physical Dependence Arm were analyzed.units on a scaleMEAN

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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GET https://conductscience.org/api/trials/v1/NCT01549652/outcomes