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NCT03841396

A Study Comparing the Local Tolerability of Two Subcutaneous Heparins in Healthy Volunteers.

Completed Phase 4 Last updated 15 February 2019
What this trial tests

Phase 4 trial testing Sodium chloride in Injection Site Reaction in 15 participants. Completed in 15 July 2016.

Timeline
2 June 2016
Primary endpoint
15 July 2016
15 July 2016

Quick facts

Lead sponsorAspen Global Incorporated
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingdouble
Primary purposeother
Enrollment15
Start date2 June 2016
Primary completion15 July 2016
Estimated completion15 July 2016

Drugs / interventions tested

Conditions studied

Sponsor

Aspen Global Incorporated

Who can join

Adults 18 to 55, any sex, with Injection Site Reaction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A Phase IV, Randomised, Double-blind, Single-centre clinical trial in healthy male and female participants aged 18 to 55, that was designed to assess and compare the pain intensity at an injection site as well as the duration of pain following a single dose subcutaneous administration of two low molecular weight heparins (LMWH) respectively.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Sodium chloride

Trials testing the same drug.

Other Aspen Global Incorporated trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03841396.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing