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
Cite this record
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
On this page
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.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Fasting Plasma Glucose (FPG) | Week 12. | Reflect the fasting glucose level after a 10- to 12-h overnight fast. |
| Primary | 2 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. |
| Primary | Glycated 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. |
| Primary | Total Insulin Secretion | Week 12. | After intervention. Total insulin secretion was calculated with the Insulinogenic index (Δ ABC insulin / Δ ABC glucose). |
| Primary | First Phase of Insulin Secretion | Week 12. | After intervention with Stumvoll index |
| Primary | Insulin Sensitivity | Week 12. | After intervention Matsuda Index |
| Secondary | Area Under the Curve of Glucose | Week 12. | Area under the curve of glucose was obtained using the trapezoidal integration. |
| Secondary | Area Under the Curve of Insulin | Week 12. | Before and after intervention area under the curve of insulin |
| Secondary | Body Weight | Week 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 |
| Secondary | Body Mass Index | Week 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 |
1 to 10 of 22Source ClinicalTrials.gov
See all 22 registered outcomesOutcomes22
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Fasting Plasma Glucose (FPG) | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | mmol/L | MEDIAN |
| PRIMARY | 2 Hours Plasma Glucose (2-h PG) | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | mmol/L | MEAN |
| PRIMARY | Glycated Hemoglobin A1c (A1C) | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | Percentage of A1C | MEAN |
| PRIMARY | Total Insulin Secretion | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | Unitless | MEAN |
| PRIMARY | First Phase of Insulin Secretion | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | Unitless | MEAN |
| PRIMARY | Insulin Sensitivity | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | Unitless | MEAN |
| SECONDARY | Area Under the Curve of Glucose | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | mmol/l/min | MEAN |
| SECONDARY | Area Under the Curve of Insulin | Week 12. | pmol/L/min | MEAN | |
| SECONDARY | Body Weight | Week 12. | 3 and 1 subjects dropout in the placebo and chlorogenic acid group respectively. | kg | MEAN |
| SECONDARY | Body Mass Index | Week 12. | kg/m^2 | MEAN |
1 to 10 of 22Source ClinicalTrials.gov
See all 22 outcomesResults by group44
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Fasting Plasma Glucose (FPG) | Placebo | 5.8 | Standard Deviation 0.3 | mmol/L | |
| Fasting Plasma Glucose (FPG) | Chlorogenic Acid | 5.5 | Standard Deviation 0.4 | mmol/L | |
| 2 Hours Plasma Glucose (2-h PG) | Placebo | 9.0 | Standard Deviation 0.8 | mmol/L | |
| 2 Hours Plasma Glucose (2-h PG) | Chlorogenic Acid | 8.5 | Standard Deviation 0.4 | mmol/L | |
| Glycated Hemoglobin A1c (A1C) | Placebo | 5.8 | Standard Deviation 0.3 | Percentage of A1C | |
| Glycated Hemoglobin A1c (A1C) | Chlorogenic Acid | 5.5 | Standard Deviation 0.4 | Percentage of A1C | |
| Total Insulin Secretion | Placebo | 0.55 | Standard Deviation 0.26 | Unitless | |
| Total Insulin Secretion | Chlorogenic Acid | 0.63 | Standard Deviation 0.25 | Unitless | |
| First Phase of Insulin Secretion | Placebo | 1281 | Standard Deviation 818 | Unitless | |
| First Phase of Insulin Secretion | Chlorogenic Acid | 1133 | Standard Deviation 601 | Unitless |
1 to 10 of 44Source ClinicalTrials.gov
See all 44 results by groupParticipant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Placebo | 15 | |
| Overall Study | STARTED | Chlorogenic Acid | 15 | |
| Overall Study | COMPLETED | Placebo | 12 | |
| Overall Study | COMPLETED | Chlorogenic Acid | 14 | |
| Overall Study | NOT COMPLETED | Placebo | 3 | |
| Overall Study | NOT COMPLETED | Chlorogenic Acid | 1 |
Source ClinicalTrials.gov
Adverse events10
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Diarrea | Gastrointestinal disorders | Placebo | 3 | 15 | |
| other | Diarrea | Gastrointestinal disorders | Chlorogenic Acid | 1 | 15 | |
| other | Headacha | Nervous system disorders | Placebo | 0 | 15 | |
| other | Headacha | Nervous system disorders | Chlorogenic Acid | 2 | 15 | |
| other | polyuria | Renal and urinary disorders | Placebo | 2 | 15 | |
| other | polyuria | Renal and urinary disorders | Chlorogenic Acid | 1 | 15 | |
| other | abdominal pain | Gastrointestinal disorders | Placebo | 1 | 15 | |
| other | abdominal pain | Gastrointestinal disorders | Chlorogenic Acid | 1 | 15 | |
| other | abdominal distention | Gastrointestinal disorders | Placebo | 1 | 15 | |
| other | abdominal distention | Gastrointestinal disorders | Chlorogenic Acid | 0 | 15 |
Source ClinicalTrials.gov
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Placebo | ||
| Total, all-cause mortality | Chlorogenic Acid | ||
| Total, other adverse events | Placebo | 3 | 15 |
| Total, other adverse events | Chlorogenic Acid | 2 | 15 |
| Total, serious adverse events | Placebo | 0 | 15 |
| Total, serious adverse events | Chlorogenic Acid | 0 | 15 |
Source ClinicalTrials.gov
Papers12
The papers the trial lists on ClinicalTrials.gov.
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 |
Source Trial comparisons
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.
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