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Trial · NCT02621060

Effect of Chlorogenic Acid on Patients With Impaired Glucose Tolerance

NCT02621060, Phase 2, Completed, University of Guadalajara; results first posted 2019-08-02

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effect of Chlorogenic Acid on Patients With Impaired Glucose Tolerance. Trials, record NCT02621060. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02621060

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Effect of Chlorogenic Acid on Patients With Impaired Glucose Tolerance
NCT number
NCT02621060
Status
Completed
Phases
Phase 2
Enrollment
30 participants, actual
Lead sponsor
University of Guadalajara
Conditions
Impaired Glucose Tolerance
Interventions
Placebo, Chlorogenic acid
First posted
2015-12-03
Last updated
2019-08-02
Results first posted
2019-08-02

Source ClinicalTrials.gov

Registered outcomes22

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryFasting Plasma Glucose (FPG)Week 12.Reflect the fasting glucose level after a 10- to 12-h overnight fast.
Primary2 Hours Plasma Glucose (2-h PG)Week 12.Subjects underwent a 2-h oral glucose tolerance test (2-h OGTT) by consuming 75-g of a dextrose load, and one sample was obtained 120 min after glucose administration.
PrimaryGlycated Hemoglobin A1c (A1C)Week 12.Shows what a person's average blood glucose level was for the 2 to 3 months before the test high-performance.
PrimaryTotal Insulin SecretionWeek 12.After intervention. Total insulin secretion was calculated with the Insulinogenic index (Δ ABC insulin / Δ ABC glucose).
PrimaryFirst Phase of Insulin SecretionWeek 12.After intervention with Stumvoll index
PrimaryInsulin SensitivityWeek 12.After intervention Matsuda Index
SecondaryArea Under the Curve of GlucoseWeek 12.Area under the curve of glucose was obtained using the trapezoidal integration.
SecondaryArea Under the Curve of InsulinWeek 12.Before and after intervention area under the curve of insulin
SecondaryBody WeightWeek 12.The weight was measured at baseline, week 4, week 8 and week 12 with a bioimpedance balance and the entered values reflect the weight at week 12
SecondaryBody Mass IndexWeek 12.The Body Mass index was calculated at baseline and at week 12 with the Quetelet index and the entered values reflect the body mass index at week 12

Outcomes22

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYFasting Plasma Glucose (FPG)Week 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.mmol/LMEDIAN
PRIMARY2 Hours Plasma Glucose (2-h PG)Week 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.mmol/LMEAN
PRIMARYGlycated Hemoglobin A1c (A1C)Week 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.Percentage of A1CMEAN
PRIMARYTotal Insulin SecretionWeek 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.UnitlessMEAN
PRIMARYFirst Phase of Insulin SecretionWeek 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.UnitlessMEAN
PRIMARYInsulin SensitivityWeek 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.UnitlessMEAN
SECONDARYArea Under the Curve of GlucoseWeek 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.mmol/l/minMEAN
SECONDARYArea Under the Curve of InsulinWeek 12.pmol/L/minMEAN
SECONDARYBody WeightWeek 12.3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively.kgMEAN
SECONDARYBody Mass IndexWeek 12.kg/m^2MEAN

Results by group44

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Fasting Plasma Glucose (FPG)Placebo5.8Standard Deviation 0.3mmol/L
Fasting Plasma Glucose (FPG)Chlorogenic Acid5.5Standard Deviation 0.4mmol/L
2 Hours Plasma Glucose (2-h PG)Placebo9.0Standard Deviation 0.8mmol/L
2 Hours Plasma Glucose (2-h PG)Chlorogenic Acid8.5Standard Deviation 0.4mmol/L
Glycated Hemoglobin A1c (A1C)Placebo5.8Standard Deviation 0.3Percentage of A1C
Glycated Hemoglobin A1c (A1C)Chlorogenic Acid5.5Standard Deviation 0.4Percentage of A1C
Total Insulin SecretionPlacebo0.55Standard Deviation 0.26Unitless
Total Insulin SecretionChlorogenic Acid0.63Standard Deviation 0.25Unitless
First Phase of Insulin SecretionPlacebo1281Standard Deviation 818Unitless
First Phase of Insulin SecretionChlorogenic Acid1133Standard Deviation 601Unitless

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPlacebo15
Overall StudySTARTEDChlorogenic Acid15
Overall StudyCOMPLETEDPlacebo12
Overall StudyCOMPLETEDChlorogenic Acid14
Overall StudyNOT COMPLETEDPlacebo3
Overall StudyNOT COMPLETEDChlorogenic Acid1

Adverse events10

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherDiarreaGastrointestinal disordersPlacebo315
otherDiarreaGastrointestinal disordersChlorogenic Acid115
otherHeadachaNervous system disordersPlacebo015
otherHeadachaNervous system disordersChlorogenic Acid215
otherpolyuriaRenal and urinary disordersPlacebo215
otherpolyuriaRenal and urinary disordersChlorogenic Acid115
otherabdominal painGastrointestinal disordersPlacebo115
otherabdominal painGastrointestinal disordersChlorogenic Acid115
otherabdominal distentionGastrointestinal disordersPlacebo115
otherabdominal distentionGastrointestinal disordersChlorogenic Acid015

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo
Total, all-cause mortalityChlorogenic Acid
Total, other adverse eventsPlacebo315
Total, other adverse eventsChlorogenic Acid215
Total, serious adverse eventsPlacebo015
Total, serious adverse eventsChlorogenic Acid015

Papers12

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
10097917BACKGROUNDPubMed
11208940BACKGROUNDPubMed
15694706BACKGROUNDPubMed
16551305BACKGROUNDPubMed
17364278BACKGROUNDPubMed
18370832BACKGROUNDPubMed
18996826BACKGROUNDPubMed
22079683BACKGROUNDPubMed
23598536BACKGROUNDPubMed
24039147BACKGROUNDPubMed

1 to 10 of 12

See all 12 papers

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Chlorogenic Acid vs Placebo: serious adverse events

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02621060

GET https://conductscience.org/api/trials/v1/NCT02621060/registered?page=2