NCT02984306

Brief Summary

Examining the effect of four weeks of cherry powder supplementation on flow mediated dilatation

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
12

participants targeted

Target at below P25 for not_applicable healthy

Timeline
Completed

Started Feb 2012

Longer than P75 for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2012

Completed
4.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2016

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2016

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

December 2, 2016

Completed
4 days until next milestone

First Posted

Study publicly available on registry

December 6, 2016

Completed
Last Updated

December 6, 2016

Status Verified

December 1, 2016

Enrollment Period

4.2 years

First QC Date

December 2, 2016

Last Update Submit

December 2, 2016

Conditions

Healthy

Outcome Measures

Primary Outcomes (1)

  • Flow mediated dilatation

    change from baseline to 4 weeks dietary supplementation

Secondary Outcomes (2)

  • Plasma nitrite concentration

    change from baseline to 4 weeks dietary supplementation

  • Plasma nitrate concentration

    change from baseline to 4 weeks dietary supplementation

Study Arms (1)

Dietary supplement

EXPERIMENTAL
Dietary Supplement: Cherry powderDietary Supplement: Placebo

Interventions

Cherry powderDIETARY_SUPPLEMENT
Dietary supplement
PlaceboDIETARY_SUPPLEMENT
Dietary supplement

Eligibility Criteria

Age40 Years - 60 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • physically inactive no prescription medications

You may not qualify if:

  • physically active taking prescription medication

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sport & Health Sciences

Exeter, Devon, EX1 2LU, United Kingdom

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 2, 2016

First Posted

December 6, 2016

Study Start

February 1, 2012

Primary Completion

May 1, 2016

Study Completion

September 1, 2016

Last Updated

December 6, 2016

Record last verified: 2016-12

Data Sharing

IPD Sharing
Will not share

Locations

GB(1)