ConductScience.org, home

Comparison · NCT03278886-deaths

Low Dose Naltrexone vs Nalmefene: deaths from any cause

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Low Dose Naltrexone vs Nalmefene: deaths from any cause. Trial comparisons, record NCT03278886-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03278886-deaths

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 1000.324wilson
Risk in group 200.00000000000000005550.561wilson
Risk difference, group 1 minus group 20-0.5610.324newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Low Dose NaltrexoneParticipants randomized to this group will receive low dose naltrexone (4.5 mg) for 8 weeks.~Low dose naltrexone: 4.5 mg of low dose naltrexone taken once daily for 8 weeks08EG000
Group 2NalmefeneParticipants randomized to this group will receive nalmefene (18 mg) for 8 weeks.~Nalmefene: 18 mg of nalmefene taken once daily for 8 weeks03EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse event data were collected over the course of the 8-week treatment period.

Source ClinicalTrials.gov

Trial

Title
St. PETERsburg Pain and Alcohol Intervention With Naltrexone and Nalmefene
NCT number
NCT03278886
Phases
PHASE1, PHASE2
Conditions
HIV Infection, Alcohol Use, Pain
Interventions
Low dose naltrexone, Nalmefene
Lead sponsor
Boston Medical Center
Results first posted
2020-08-03

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT03278886-deaths