NCT01738763 is a NA clinical trial of Pinitol in Healthy, sponsored by University of Valencia.

Who is sponsoring NCT01738763?

NCT01738763 is sponsored by University of Valencia.

What drugs are being tested in NCT01738763?

Interventions in NCT01738763: Pinitol.

What condition does NCT01738763 study?

NCT01738763 studies Healthy, Insulin Sensitivity.

Is NCT01738763 still recruiting?

NCT01738763 is currently completed. Last updated 27 November 2012.

Last reviewed 2012-11-27 · How we verify

NCT01738763

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

Effects of Different Doses of Pinitol on Carbohydrate Metabolism Parameters in Healthy Subjects: a Randomized Cross-over Placebo-controlled Study

Completed NA Last updated 27 November 2012

What this trial tests

NA trial testing Pinitol in Healthy in 30 participants. Completed in 1 January 2012.

Timeline

1 July 2011

Primary endpoint
1 November 2011

1 January 2012

Quick facts

Lead sponsor	University of Valencia
Phase	NA
Status	Completed
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	single
Primary purpose	basic science
Enrollment	30
Start date	1 July 2011
Primary completion	1 November 2011
Estimated completion	1 January 2012
Sites	1 location across Spain

Drugs / interventions tested

Pinitol

Conditions studied

Healthy — all drugs for Healthy →
Insulin Sensitivity — all drugs for Insulin Sensitivity →

Sponsor

University of Valencia

Who can join

Adults 18 to 65, any sex, with Healthy or Insulin Sensitivity. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Dose-response curves to assess the change in glucose and insulin concentration after an oral ingestion of different doses of pinitol with respect to the corresponding placebo
Time frame: up to 120 minutes
Each subject attended the Endocrinology Service in the morning after 12-hour overnight fasting. Blood sample was collected in vacutainer serum separator tubes at baseline (minute 0; while still fasting), 15, 30, 45, 60, 90 and 120 minutes after consumption of the tested product placebo or pinitol-enriched beverage. Glucose concentrations were measured by means of enzymatic assay in an autoanalyzer

Sponsor's own description

The purpose of this study was to assess the acute effects of increasing doses of pinitol on glucose tolerance and insulin sensitivity and to evaluate the absorption of pinitol after consumption of an oral nutritive pinitol-enriched beverage in healthy subjects.

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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Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT01738763 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by University of Valencia
Last refreshed: 27 November 2012

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/NCT01738763.

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