Periodontal DiseasesNCT06184412
Periodontal Status and Endothelial Dysfunction in Patients With Polycystic Ovary Syndrome
An observational study of Periodontal Diseases, run by Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana at 1 site in Spain.
Trial summary
Emerging research indicates a link between polycystic ovary syndrome (PCOS) and periodontal diseases, revealing the intricate relationship between oral health and systemic conditions. Read more about this study
- Who is it for?
- Ages 18 to 45 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Periodontal Diseases
- How many people
- 100 participants
- Where
- 1 siteSpain
- Study dates
- 1 Feb 2020to 1 Sep 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 45 years
- Women only
- Healthy volunteers accepted
- Adult
Study population: Primary care clinic
Who may be able to join
- Women with polycystic ovary syndrome (PCOS) according to the Rotterdam criteria:
- Irregular ovulation (cycles longer than 35 days or less than 26 days)
- Elevated levels of free testosterone (>0.5 ng/dl)
- Hirsutism and the presence of polycystic ovaries
- Healthy women without periodontal diseases matched in BMI and age to the PCOS group.
Who cannot join
- Other systemic inflammatory conditions
- Recent antibiotic use
- Chronic anti-inflammatory use
- Cancerous or bone-affecting pathologies
- Diabetes or autoimmune diseases
- Use of any medication during the previous semester
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Periodontal Status Assessment, Molecular Mechanisms Underlying Inflammatory Response, and Endothelial Dysfunction Evaluation in Patients With Polycystic Ovary Syndrome
Emerging research indicates a link between polycystic ovary syndrome (PCOS) and periodontal diseases, revealing the intricate relationship between oral health and systemic conditions. PCOS, a hormonal disorder in women of reproductive age, often associates with obesity, dyslipidemia, and insulin resistance, heightening the risk for type 2 diabetes (T2D) and cardiovascular disease (CVD). The pathogenesis of PCOS involves an inflammatory response marked by increased CRP, inflammatory cytokines, elevated blood leukocytes, adhesion molecule expression, and oxidative stress markers like myeloperoxidase (MPO).
Periodontal diseases, bacterial infections affecting gums, ligaments, cement, and bone, include gingivitis (gum inflammation) and periodontitis (irreversible tissue destruction). Evidence suggests a link between periodontitis and increased CVD risk, while such association with gingivitis is limited.
Read more
Potential mechanisms linking periodontal diseases and CVD involve cytokine release, oral bacteria toxin production, and direct bloodstream transfer. Recognition of lipopolysaccharide (LPS) and TNFα triggers innate immune cells via TLR4 and TNFR, activating NF-κB and JNK expression. JNK amplifies inflammatory responses, inducing proinflammatory genes, and TNFα, IL-1, IL-6, and IL-8 can invade endothelial layers, promoting adhesion molecule expression. Enhanced leukocyte ROS production, especially in periodontitis, contributes to endothelial dysfunction and heightened cardiovascular risk.
The activation of multiple inflammatory pathways likely links PCOS, periodontal disease, and increased cardiovascular risk. Thus, the researchers aim to investigate if the presence of periodontal diseases, particularly gingivitis, exacerbates oxidative stress, inflammation and atherosclerosis surrogate markers in women with PCOS, and explore the underlying molecular mechanisms.
Read the detailed description
The population will be identified using the Rotterdam criteria, which will include the following characteristics: irregular ovulation (cycles longer than 35 days or less than 26 days); elevated levels of free testosterone (>0.5 ng/dl; the cut-off level for free testosterone will be determined based on the mean ± 2 standard deviations from normal levels observed in the control group); hirsutism (total Ferriman-Gallwey score > 7); and the presence of polycystic ovaries, which will be identified through transvaginal ultrasonography (i.e., the presence of 12 or more small follicles measuring 2 to 9 mm in each ovary). The control group will be matched in BMI and age to the intervention group. In both groups, all medication, pathologies, and other medical conditions that could affect their reproductive physiology will be registered. All patients will receive detailed information on the study, highlighting its benefits and drawbacks, and will sign the informed consent and confidentiality commitment.
A comprehensive periodontal examination will be conducted across all study cohorts, adhering to established consensus criteria. Each tooth in the oral cavity will be probed at 6 points-3 buccal and 3 palatal-utilizing a periodontal chart with a Williams-type millimeter probe. Factors such as tobacco use, tooth brushing frequency, and alcohol consumption will be considered via a questionnaire, as well as through plaque and calculus indices. The periodontal examination will be carried out by a single doctor with training in periodontics to avoid inter-explorer bias. The researchers will also ask about dental treatments received, emphasizing periodontal treatments or those related to generating changes in soft tissues such as orthodontic gingival recessions. The periodontal measures will include the percentage of bleeding on probing (BOP), millimeters of clinical attachment level (CAL), millimeters of probing pockets depth (PPD), percentage of loss of bone, number of teeth with periodontal pockets-PPD ≥4mm- and number of teeth with CAL≥4mm-. The researchers will evaluate the plaque and calculus level using the Silness and Löe index for plaque and O´Leary index for calculus levels. To facilitate the measurement of plaque and calculus indexes, as they will be carried out in a hospital with a high flux of patients, these indices will be measured on the Ramfjord index teeth (right permanent maxillary first molar, right permanent incisor, left permanent first premolar, left mandibular permanent first molar, right permanent mandibular incisor, and right permanent mandibular first premolar).
A peripheral venous blood sample will be taken after 12 hours of fasting, during the follicular phase of the menstrual period of the patients (from the 1st to the 5th day of bleeding) to avoid biases dependent on the variability of sexual hormones. Neutrophils and PBMC will be isolated from 8 mL of EDTA-anticoagulated peripheral blood by means of an immunomagnetic method, following the manufacturer's protocol. In addition, LUNA-FL will be used to determine cell count and viability (acridine orange and propidium iodide double stain). Proteins will be extracted from neutrophils or PBMC on ice. Neutrophils will be lysed for 15 minutes with RIPA Lysis Buffer supplemented with protease and phosphatase inhibitors. The supernatant will be collected after centrifugation for 15 minutes at 16,000g. The total protein concentration will be quantified using a bicinchoninic acid (BCA) protein assay. Aliquots of 25µg of protein will be resolved on 8-16% gradient SDS-polyacrylamide gels and transferred to nitrocellulose membranes. Target proteins will be detected by incubating the membranes with anti-actin, JNK, NFkB, MCP1, GPX-1, NLRP3, ASC, procaspase 1, caspase 1, Beclin, ATG5-ATG12, p62, LC3 I, LC3 II, Pink1, GRP78, eIF2alpha, IRE1 alpha, ATF6, CHOP, PGC1 alpha, mTFA, VDAC, Complex I, II, III, IV and V. The protein signal will be detected by chemiluminescence and analyzed by densitometry.
A parallel plate flow chamber, connected to an inverted microscope, will enable the researchers to measure neutrophil-endothelial cell interactions in vitro. Prior to this, immortalized endothelial cells from the human umbilical vein will be seeded. One million leukocytes in 1 mL of RPMI medium will be drawn across the HUVEC. A video camera connected to the microscope will permit a 5 × 25 mm view of the endothelial cells. Various leukocyte parameters, including rolling velocity, rolling flux, and adhesion, will be evaluated over a period of 5 minutes. Analysis of serum cytokines, cellular adhesion molecules, and glutathione will be measured with a Luminex® 200 analyzer system following the Milliplex® MAP Kit manufacturer's procedure or ELISA technique.
This study was designed to achieve a power of 80% and to detect significant differences of 20 % in relation to the primary efficacy criterion - leukocyte-endothelium interactions (measured by adhesion of neutrophils) - assuming that 3 groups existed. Under these premises, at least 12 subjects per group were considered. Normally and non-normally distributed data will be expressed as mean ± standard deviation (SD) and median (25th-75th percentiles), respectively. Qualitative data will be expressed as percentages. The data will be analyzed using an unpaired Student's t test or a Mann-Whitney U test for parametric and non-parametric data, respectively. When comparing three groups, statistical significance will be assessed by one-way ANOVA or the Kruskal Wallis test followed by post hoc test. The strength of the association between variables will be measured by means of Pearson's or Spearman correlation coefficient, for parametric and non-parametric data, respectively. To predict the value of a variable based on another variable, linear regression analysis will be used. Differences will be considered significant when p < 0.05, with a confidence interval of 95%. Analysis will be performed with SPSS 22.0.
- Conditions
- Periodontal Diseases
- Keywords
- inflammation, atherosclerosis, gingivitis, oxidative stress
- Medical subject headings
- Periodontal Diseases, Inflammation, Atherosclerosis, Gingivitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Control group without periodontal disease | Women without periodontal disease neither PCOS | |
| PCOS group with or without periodontal disease | Women with PCOS with or without periodontal disease |
What is being measured
The primary outcome is the main question the study is designed to answer.
Evaluate subclinical atherosclerotic markers in the study population
Determine leukocyte-endothelial cell interactions and cellular adhesion molecules in serum (ICAM, VCAM and p-Selectin)
Measured: At recruitment
Evaluate inflammatory markers in the study population
Determine proinflammatory cytokines in serum (TNF-alpha, IL6) and expression of inflammatory mediators in leukocytes by Western blot (JNK, NFkB, MCP1)
Measured: At recruitment
Evaluate oxidative stress markers in the study population
Determine serum oxidative stress markers (MPO, glutathione), expression of GPX-1 by Western blot and total ROS, mitochondrial ROS and superoxide by flow cytometry in leukocytes.
Measured: At recruitment
Secondary outcomes (4)
Evaluate inflammasome complex activation in the study population
Determine expression of NLRP3, ASC, procaspase 1 and caspase 1 by Western blot in leukocytes and serum levels of IL1 beta and IL18 in serum.
Measured: At recruitment
Evaluate markers of autophagy in the study population
Determine expression of Beclin, ATG5-ATG12, p62, LC3 I, LC3 II and Pink by Western blot in leukocytes.
Measured: At recruitment
Evaluate markers of ER stress in the study population
Determine expression of GRP78, eIF2alpha, IRE1 alpha, ATF6 and CHOP by Western blot in leukocytes.
Measured: At recruitment
Evaluate markers of mitochondrial biogenesis and complexes in the study population
Determine expression of PGC1 alpha, mTFA, VDAC, Complex I, II, III, IV and V by Western blot in leukocytes.
Measured: At recruitment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Dec 2023
- Study start1 Feb 2020
- Primary completion1 Jun 2022
- Study completion1 Sep 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (7)Papers the sponsor has linked to this study.
- Other trials for Periodontal DiseasesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
- Sponsor type
- University, hospital or other
- Collaborators
- Instituto de Salud Carlos III
- Responsible party
- Principal investigator, Milagros Rocha Barajas, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
- Investigators
- Milagros Rocha, PhD, Principal investigator, FISABIO-HOSPITAL DR PESET
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06184412
- Sponsor's protocol ID
- PI19/00437B
- Status last verified
- Jan 2024
- First submitted
- 14 Dec 2023
- Last updated
- 9 Jan 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Marquez-Arrico CF, Silvestre-Rangil J, Gutierrez-Castillo L, Martinez-Herrera M, Silvestre FJ, Rocha M. Association between Periodontal Diseases and Polycystic Ovary Syndrome: A Systematic Review. J Clin Med. 2020 May 23;9(5):1586. doi: 10.3390/jcm9051586.
PubMed 32456146Romandini M, Baima G, Antonoglou G, Bueno J, Figuero E, Sanz M. Periodontitis, Edentulism, and Risk of Mortality: A Systematic Review with Meta-analyses. J Dent Res. 2021 Jan;100(1):37-49. doi: 10.1177/0022034520952401. Epub 2020 Aug 31.
PubMed 32866427Porwal S, Tewari S, Sharma RK, Singhal SR, Narula SC. Periodontal status and high-sensitivity C-reactive protein levels in polycystic ovary syndrome with and without medical treatment. J Periodontol. 2014 Oct;85(10):1380-9. doi: 10.1902/jop.2014.130756. Epub 2014 Mar 4.
PubMed 24592911Schenkein HA, Loos BG. Inflammatory mechanisms linking periodontal diseases to cardiovascular diseases. J Clin Periodontol. 2013 Apr;40 Suppl 14(0 14):S51-69. doi: 10.1111/jcpe.12060.
PubMed 23627334Greabu M, Giampieri F, Imre MM, Mohora M, Totan A, Pituru SM, Ionescu E. Autophagy, One of the Main Steps in Periodontitis Pathogenesis and Evolution. Molecules. 2020 Sep 22;25(18):4338. doi: 10.3390/molecules25184338.
PubMed 32971808Domon H, Takahashi N, Honda T, Nakajima T, Tabeta K, Abiko Y, Yamazaki K. Up-regulation of the endoplasmic reticulum stress-response in periodontal disease. Clin Chim Acta. 2009 Mar;401(1-2):134-40. doi: 10.1016/j.cca.2008.12.007. Epub 2008 Dec 13.
PubMed 19109937Paladines N, Dawson S, Ryan W, Serrano-Lopez R, Messer R, Huo Y, Cutler CW, Ramos-Junior ES, Morandini AC. Metabolic reprogramming through mitochondrial biogenesis drives adenosine anti-inflammatory effects: new mechanism controlling gingival fibroblast hyper-inflammatory state. Front Immunol. 2023 Jun 7;14:1148216. doi: 10.3389/fimmu.2023.1148216. eCollection 2023.
PubMed 37350964
Study at a glance
From the registry record, last updated by the sponsor on 9 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Periodontal Status Assessment, Molecular Mechanisms Underlying Inflammatory Response, and Endothelial Dysfunction Evaluation in Patients With Polycystic Ovary Syndrome
- ClinicalTrials.gov ID
- NCT06184412
- Acronym / sponsor ID
- PI19/00437B
- Conditions
- Periodontal Diseases
- Keywords
- inflammation, atherosclerosis, gingivitis, oxidative stress
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat ValencianaUniversity, hospital or other
- Collaborators
- Instituto de Salud Carlos III
- Study start
- 1 Feb 2020 (actual)
- Primary completion
- 1 Jun 2022 (actual)
- Study completion
- 1 Sep 2022 (actual)
- First posted
- 28 Dec 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Emerging research indicates a link between polycystic ovary syndrome (PCOS) and periodontal diseases, revealing the intricate relationship between oral health and systemic conditions. PCOS, a hormonal disorder in women of reproductive age, often associates with obesity, dyslipidemia, and insulin resistance, heightening the risk for type 2 diabetes (T2D) and cardiovascular disease (CVD). The pathogenesis of PCOS involves an inflammatory response marked by increased CRP, inflammatory cytokines, elevated blood leukocytes, adhesion molecule expression, and oxidative stress markers like myeloperoxidase (MPO).
Periodontal diseases, bacterial infections affecting gums, ligaments, cement, and bone, include gingivitis (gum inflammation) and periodontitis (irreversible tissue destruction). Evidence suggests a link between periodontitis and increased CVD risk, while such association with gingivitis is limited.
Potential mechanisms linking periodontal diseases and CVD involve cytokine release, oral bacteria toxin production, and direct bloodstream transfer. Recognition of lipopolysaccharide (LPS) and TNFα triggers innate immune cells via TLR4 and TNFR, activating NF-κB and JNK expression. JNK amplifies inflammatory responses, inducing proinflammatory genes, and TNFα, IL-1, IL-6, and IL-8 can invade endothelial layers, promoting adhesion molecule expression. Enhanced leukocyte ROS production, especially in periodontitis, contributes to endothelial dysfunction and heightened cardiovascular risk.
The activation of multiple inflammatory pathways likely links PCOS, periodontal disease, and increased cardiovascular risk. Thus, the researchers aim to investigate if the presence of periodontal diseases, particularly gingivitis, exacerbates oxidative stress, inflammation and atherosclerosis surrogate markers in women with PCOS, and explore the underlying molecular mechanisms.
Detailed description
The population will be identified using the Rotterdam criteria, which will include the following characteristics: irregular ovulation (cycles longer than 35 days or less than 26 days); elevated levels of free testosterone (>0.5 ng/dl; the cut-off level for free testosterone will be determined based on the mean ± 2 standard deviations from normal levels observed in the control group); hirsutism (total Ferriman-Gallwey score > 7); and the presence of polycystic ovaries, which will be identified through transvaginal ultrasonography (i.e., the presence of 12 or more small follicles measuring 2 to 9 mm in each ovary). The control group will be matched in BMI and age to the intervention group. In both groups, all medication, pathologies, and other medical conditions that could affect their reproductive physiology will be registered. All patients will receive detailed information on the study, highlighting its benefits and drawbacks, and will sign the informed consent and confidentiality commitment.
A comprehensive periodontal examination will be conducted across all study cohorts, adhering to established consensus criteria. Each tooth in the oral cavity will be probed at 6 points-3 buccal and 3 palatal-utilizing a periodontal chart with a Williams-type millimeter probe. Factors such as tobacco use, tooth brushing frequency, and alcohol consumption will be considered via a questionnaire, as well as through plaque and calculus indices. The periodontal examination will be carried out by a single doctor with training in periodontics to avoid inter-explorer bias. The researchers will also ask about dental treatments received, emphasizing periodontal treatments or those related to generating changes in soft tissues such as orthodontic gingival recessions. The periodontal measures will include the percentage of bleeding on probing (BOP), millimeters of clinical attachment level (CAL), millimeters of probing pockets depth (PPD), percentage of loss of bone, number of teeth with periodontal pockets-PPD ≥4mm- and number of teeth with CAL≥4mm-. The researchers will evaluate the plaque and calculus level using the Silness and Löe index for plaque and O´Leary index for calculus levels. To facilitate the measurement of plaque and calculus indexes, as they will be carried out in a hospital with a high flux of patients, these indices will be measured on the Ramfjord index teeth (right permanent maxillary first molar, right permanent incisor, left permanent first premolar, left mandibular permanent first molar, right permanent mandibular incisor, and right permanent mandibular first premolar).
A peripheral venous blood sample will be taken after 12 hours of fasting, during the follicular phase of the menstrual period of the patients (from the 1st to the 5th day of bleeding) to avoid biases dependent on the variability of sexual hormones. Neutrophils and PBMC will be isolated from 8 mL of EDTA-anticoagulated peripheral blood by means of an immunomagnetic method, following the manufacturer's protocol. In addition, LUNA-FL will be used to determine cell count and viability (acridine orange and propidium iodide double stain). Proteins will be extracted from neutrophils or PBMC on ice. Neutrophils will be lysed for 15 minutes with RIPA Lysis Buffer supplemented with protease and phosphatase inhibitors. The supernatant will be collected after centrifugation for 15 minutes at 16,000g. The total protein concentration will be quantified using a bicinchoninic acid (BCA) protein assay. Aliquots of 25µg of protein will be resolved on 8-16% gradient SDS-polyacrylamide gels and transferred to nitrocellulose membranes. Target proteins will be detected by incubating the membranes with anti-actin, JNK, NFkB, MCP1, GPX-1, NLRP3, ASC, procaspase 1, caspase 1, Beclin, ATG5-ATG12, p62, LC3 I, LC3 II, Pink1, GRP78, eIF2alpha, IRE1 alpha, ATF6, CHOP, PGC1 alpha, mTFA, VDAC, Complex I, II, III, IV and V. The protein signal will be detected by chemiluminescence and analyzed by densitometry.
A parallel plate flow chamber, connected to an inverted microscope, will enable the researchers to measure neutrophil-endothelial cell interactions in vitro. Prior to this, immortalized endothelial cells from the human umbilical vein will be seeded. One million leukocytes in 1 mL of RPMI medium will be drawn across the HUVEC. A video camera connected to the microscope will permit a 5 × 25 mm view of the endothelial cells. Various leukocyte parameters, including rolling velocity, rolling flux, and adhesion, will be evaluated over a period of 5 minutes. Analysis of serum cytokines, cellular adhesion molecules, and glutathione will be measured with a Luminex® 200 analyzer system following the Milliplex® MAP Kit manufacturer's procedure or ELISA technique.
This study was designed to achieve a power of 80% and to detect significant differences of 20 % in relation to the primary efficacy criterion - leukocyte-endothelium interactions (measured by adhesion of neutrophils) - assuming that 3 groups existed. Under these premises, at least 12 subjects per group were considered. Normally and non-normally distributed data will be expressed as mean ± standard deviation (SD) and median (25th-75th percentiles), respectively. Qualitative data will be expressed as percentages. The data will be analyzed using an unpaired Student's t test or a Mann-Whitney U test for parametric and non-parametric data, respectively. When comparing three groups, statistical significance will be assessed by one-way ANOVA or the Kruskal Wallis test followed by post hoc test. The strength of the association between variables will be measured by means of Pearson's or Spearman correlation coefficient, for parametric and non-parametric data, respectively. To predict the value of a variable based on another variable, linear regression analysis will be used. Differences will be considered significant when p < 0.05, with a confidence interval of 95%. Analysis will be performed with SPSS 22.0.
Study design
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control group without periodontal disease | – | –Women without periodontal disease neither PCOS |
| PCOS group with or without periodontal disease | – | –Women with PCOS with or without periodontal disease |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Primary care clinic
Key inclusion criteria (5 listed)
- Women with polycystic ovary syndrome (PCOS) according to the Rotterdam criteria:
- Healthy women without periodontal diseases matched in BMI and age to the PCOS group.
Key exclusion criteria (6 listed)
- Other systemic inflammatory conditions
- Recent antibiotic use
- Chronic anti-inflammatory use
- Cancerous or bone-affecting pathologies
- Diabetes or autoimmune diseases
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Evaluate subclinical atherosclerotic markers in the study population
Time frame: At recruitment
Determine leukocyte-endothelial cell interactions and cellular adhesion molecules in serum (ICAM, VCAM and p-Selectin)
Evaluate inflammatory markers in the study population
Time frame: At recruitment
Determine proinflammatory cytokines in serum (TNF-alpha, IL6) and expression of inflammatory mediators in leukocytes by Western blot (JNK, NFkB, MCP1)
Evaluate oxidative stress markers in the study population
Time frame: At recruitment
Determine serum oxidative stress markers (MPO, glutathione), expression of GPX-1 by Western blot and total ROS, mitochondrial ROS and superoxide by flow cytometry in leukocytes.
4 secondary outcomes
Evaluate inflammasome complex activation in the study population
Time frame: At recruitment
Evaluate markers of autophagy in the study population
Time frame: At recruitment
Evaluate markers of ER stress in the study population
Time frame: At recruitment
Evaluate markers of mitochondrial biogenesis and complexes in the study population
Time frame: At recruitment
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Jan 2024.
- Background: PubMed 32456146Marquez-Arrico CF, Silvestre-Rangil J, Gutierrez-Castillo L, Martinez-Herrera M, Silvestre FJ, Rocha M. Association between Periodontal Diseases and Polycystic Ovary Syndrome: A Systematic Review. J Clin Med. 2020 May 23;9(5):1586. doi: 10.3390/jcm9051586.
- Background: PubMed 32866427Romandini M, Baima G, Antonoglou G, Bueno J, Figuero E, Sanz M. Periodontitis, Edentulism, and Risk of Mortality: A Systematic Review with Meta-analyses. J Dent Res. 2021 Jan;100(1):37-49. doi: 10.1177/0022034520952401. Epub 2020 Aug 31.
- Background: PubMed 24592911Porwal S, Tewari S, Sharma RK, Singhal SR, Narula SC. Periodontal status and high-sensitivity C-reactive protein levels in polycystic ovary syndrome with and without medical treatment. J Periodontol. 2014 Oct;85(10):1380-9. doi: 10.1902/jop.2014.130756. Epub 2014 Mar 4.
- Background: PubMed 23627334Schenkein HA, Loos BG. Inflammatory mechanisms linking periodontal diseases to cardiovascular diseases. J Clin Periodontol. 2013 Apr;40 Suppl 14(0 14):S51-69. doi: 10.1111/jcpe.12060.
- Background: PubMed 32971808Greabu M, Giampieri F, Imre MM, Mohora M, Totan A, Pituru SM, Ionescu E. Autophagy, One of the Main Steps in Periodontitis Pathogenesis and Evolution. Molecules. 2020 Sep 22;25(18):4338. doi: 10.3390/molecules25184338.
- Background: PubMed 19109937Domon H, Takahashi N, Honda T, Nakajima T, Tabeta K, Abiko Y, Yamazaki K. Up-regulation of the endoplasmic reticulum stress-response in periodontal disease. Clin Chim Acta. 2009 Mar;401(1-2):134-40. doi: 10.1016/j.cca.2008.12.007. Epub 2008 Dec 13.
- Background: PubMed 37350964Paladines N, Dawson S, Ryan W, Serrano-Lopez R, Messer R, Huo Y, Cutler CW, Ramos-Junior ES, Morandini AC. Metabolic reprogramming through mitochondrial biogenesis drives adenosine anti-inflammatory effects: new mechanism controlling gingival fibroblast hyper-inflammatory state. Front Immunol. 2023 Jun 7;14:1148216. doi: 10.3389/fimmu.2023.1148216. eCollection 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Milagros Rocha, PhD principal investigator
FISABIO-HOSPITAL DR PESET
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Periodontal Diseases, run by Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana at 1 site in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 9 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Evaluate subclinical atherosclerotic markers in the study population (time frame: At recruitment). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06184412, which also lists 7 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2024.