Disease × agent evidence record

Propranolol Hydrochloride for Sepsis: evidence, trials and status

Propranolol Hydrochloride has 1 completed registered trial for Sepsis but no linked publication, which usually means results are unpublished, pending, or not yet matched to this record.

1 registered trials 0 recruiting 0 publications Evidence tier A · Strong Score 22.5
Research Tracker › Pairs › Sepsis › Propranolol Hydrochloride
Research map, not treatment advice. This page aggregates registry and literature records. It does not evaluate efficacy, dosing or safety for any individual. Discuss any treatment decision with a qualified clinician.

Summary

Propranolol Hydrochloride has reached the approved stage (maximum clinical phase 4) for at least one indication, so its use in Sepsis would be drug repurposing rather than first-in-human development. This does not mean it is approved for Sepsis. ClinicalTrials.gov lists 1 registered trial linking Propranolol Hydrochloride to Sepsis: 1 has completed. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 42 participants. Registered activity dates to 2020. No published literature item is linked to Propranolol Hydrochloride and Sepsis in the OSMF database yet, so the record rests on registry entries alone. Registry entries describe intent to study, not outcomes.

The RepurpOS disease-intelligence file for Sepsis ranks 518 candidate therapeutics from Open Targets, ChEMBL, DGIdb and PubMed; only a minority carry direct clinical evidence, and this page covers one of those. Spontaneous remission context recorded for the condition: Not applicable — sepsis is an acute life-threatening syndrome; hospital mortality 15-25% for sepsis, 30-45% for septic shock with standard care; long-term complications (post-sepsis syndrome) in 50-70% of survivors.

Evidence table

Evidence tierA · Strong
Evidence score22.5 (trials 2.5, literature 0.0, tier 15, approved bonus 5.0)
Registered trials1 total: 0 recruiting, 0 active / not yet recruiting, 1 completed, 0 other
Linked publications0
Agent typeDrug (Small molecule)
Development stage (any indication)Approved
Mechanism / classNot recorded
Data sourcesDGIdb
Linked via biomarker / targetADRA2C
How the evidence score is calculated
  • Each registered trial scores by status (recruiting / active / enrolling 3, completed 2.5, not yet recruiting 2, unknown 1, terminated / withdrawn / suspended 0.5) plus a phase bonus (phase 3-4 +2, phase 2 +1, phase 1 +0.5). The trial component is capped at 30.
  • Each literature item scores by design (Cochrane review 5, meta-analysis 4, systematic review 3, RCT 3, clinical trial publication 2, curated reference 1.5, other PubMed record 1). The literature component is capped at 30.
  • The existing evidence tier adds 15 (A / Strong), 10 (B / Moderate), 5 (C / Preliminary) or 0 (D / Anecdotal).
  • Agents approved for any indication (max clinical phase 4) add 5, because an approved agent has an established safety profile that lowers the barrier to repurposing trials.
  • The score ranks what has been studied, not what works. It does not read effect sizes or directions of effect.

Registered clinical trials

NCT IDTitleStatusPhaseEnrolment
NCT04467762Neurocognitive Impairment in Pediatric Patients With Meningoencephalitis and Sepsis-associated Encephalopathy
2020
completedNot applicable42

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Published literature

No publication is linked to this pair yet.

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Mechanism and notes

No mechanism of action is recorded for this pair in the source databases.

OSMF's existing evidence tier for this pair is A (Strong), derived from the strength of the disease association recorded in DGIdb, in this case via the biomarker or target ADRA2C. The tier describes how well the drug-disease link is documented, not how well the drug works.

Frequently asked questions

Is Propranolol Hydrochloride approved for Sepsis?

Propranolol Hydrochloride has reached the approved stage (maximum clinical phase 4) for at least one indication, so its use in Sepsis would be drug repurposing rather than first-in-human development. This does not mean it is approved for Sepsis. Approval status for the specific indication should always be confirmed with the relevant regulator and prescribing information.

Is Propranolol Hydrochloride in clinical trials for Sepsis?

ClinicalTrials.gov lists 1 registered trial linking Propranolol Hydrochloride to Sepsis: 1 has completed. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 42 participants. Registered activity dates to 2020.

What does the evidence show for Propranolol Hydrochloride in Sepsis?

Propranolol Hydrochloride has 1 completed registered trial for Sepsis but no linked publication, which usually means results are unpublished, pending, or not yet matched to this record. OSMF's existing evidence tier for this pair is A (Strong), derived from the strength of the disease association recorded in DGIdb, in this case via the biomarker or target ADRA2C. The tier describes how well the drug-disease link is documented, not how well the drug works.

Cite this page

Open Source Medicine Foundation. Propranolol Hydrochloride for Sepsis: evidence, trials and status. OSMF Research Tracker. Updated 2026-07-05. https://research.opensourcemed.info/pairs/sepsis/propranolol-hydrochloride.html

Data: ClinicalTrials.gov, PubMed, Open Targets, ChEMBL, DGIdb and the OSMF therapeutic agent database. Last updated 2026-07-05. Page built 2026-10-07.

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This is a research map, not treatment advice. Evidence tiers and scores summarise what has been studied, not whether a treatment works or is safe for you.