CI

At a glance

ClinicalIndex Comparison Record
Early Ph 1Completed· 44 enrolled
Drug / intervention
Omega-3 SPM™ softgeldietary
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02683850
NCT02683850Early Ph 1Completed

Influence of an Omega-3 SPM Supplement on Quality of Life

National University of Natural Medicine·interventional·Posted Feb 17, 2016·Updated Sep 2, 2016

In Brief

A Early Phase 1 clinical trial evaluating Omega-3 SPM™ softgel for Chronic Pain. Completed, enrolled 44 participants across 1 site.

Detailed Summary

This prospective, non-randomized, open-label study will assess if taking an Omega-3 SPM™ soft gel supplement for four weeks will increase the quality of life in adults with chronic pain.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Pain
CountriesUnited States
CollaboratorsMetagenics, Inc.

Timeline

Early Ph 1CompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 17, 2016
Enrollment StartJan 1, 2016
Primary CompletionJul 1, 2016
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 10.4 years ago

Interventions

Omega-3 SPM™ softgeldietary

This four week, prospective, non-randomized, open-label study is assessing the impact on quality of life from taking an Omega-3 SPM™ softgel supplement in adults with pain symptoms at screening of 4 or higher on the PROMIS-43 Profile - Pain Intensity subscale.