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NCT02311790 · ClinicalTrials.gov registry record · NA

Palmitoleic Isomer Study

A NA study, sponsored by Tufts University.

Completed
Registry status
NA
Development phase
17
Enrollment target

NCT02311790: Completed NA study, sponsored by Tufts University.

NCT02311790 is a NA study that has completed, run by Tufts University. The registered enrollment target is 17 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02311790, a NA study, has completed, sponsored by Tufts University.

COMPLETED
Registry status
NA
Development phase
17 participants
Enrollment target

Study Summary

Trans-palmitoleic acid (trans-C16:1) is a naturally occurring trans fatty acid present in small quantities in foods, most notably in dairy products. Observational evidence suggests a positive association between trans-C16:1 and insulin sensitivity, and negative association with risk of developing type 2 diabetes mellitus \[1-3\]. Cis-palmitoleic acid (cis-C16:1) is found naturally in foods and is particularly high in macadamia nuts and oil extracted from the sea buckthorn plant. Animal models suggest that this palmitoleic acid isomer also improves insulin sensitivity and reduces metabolic dysfunction. This pilot dosing study is necessary to inform the design of a larger trial to test the hypothesis that both trans-C16:1 and cis-C16:1 improve insulin resistance but at different doses. Plasma phospholipid fatty acid profiles will be used as the primary outcome measure.

Primary Outcome

PLP FA profile determined by gas chromatography

Interventions

  • DIETARY_SUPPLEMENT Trans-C16:1 supplement
  • DIETARY_SUPPLEMENT Cis-C16:1 supplement

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2015-07
Est. Completion 2017-04
Phase NA
Tufts University

163 total trials

What the finished NCT02311790 record still lists

NCT02311790 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Trans-C16:1 supplement is the first listed.

NCT02311790 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02311790 about?

NCT02311790 is a clinical study titled "Palmitoleic Isomer Study". Trans-palmitoleic acid (trans-C16:1) is a naturally occurring trans fatty acid present in small quantities in foods, most notably in dairy products. Observational evidence suggests a positive association between trans-C16:1 and insulin sensitivity, and negative association with risk of developing ty...

What is the current status of trial NCT02311790?

This trial is currently completed. It is a NA study. The enrollment target is 17 participants. The study started on 2015-07. Estimated completion is 2017-04.

What interventions are being tested in trial NCT02311790?

The interventions under investigation include: Trans-C16:1 supplement (DIETARY_SUPPLEMENT), Cis-C16:1 supplement (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT02311790?

This trial is sponsored by Tufts University, which has 163 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02311790's enrollment target sits among peer trials

17 1871st of 2000 higher than 130 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02311790, the US trial registry maintained by the National Library of Medicine. NCT02311790 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.