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Patients with Clinical Complaints of Fibromyalgia Among the Patients Applying to the Outpatient ClinicNCT06725199

Metabolomic Profiling Based on Nuclear Magnetic Resonance in Fibromyalgia Patients

An observational study of Patients with Clinical Complaints of Fibromyalgia Among the Patients Applying to the Outpatient Clinic and Fibromyalgia Syndrome, run by hatice kübra aşık at 1 site in Turkey (Türkiye).

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Evaluation of sera of fibromyalgia patients in terms of energy metabolism function and possible alterations in metabolism predisposing to various degenerative/proliferative diseases. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
How many people
100 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Sep 2024to Feb 2025
How long will I take part?
1 Day
Phase
Observational
Are there results?
Not yet: the study is under way

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 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: patients aged 18-65 years Patients with clinical complaints of fibromyalgia and control group (healthy)

Who may be able to join

  • patients aged 18-65 years Patients with clinical complaints of fibromyalgia

Who cannot join

  • Viral or bacterial infections, Diabetes mellitus, Hypertension, Chronic renal failure, Hypo-hyperthyroidism) Patients taking antidepressants or medication, Smokers and alcohol users, Patients with rheumatic arthritis and systemic lupus erythematosus were excluded.
  • -

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Turkey (Türkiye)1 site
  • University of Beykent

    Istanbul, Istanbul, 34000

Other trials in Turkey (Türkiye)

About this study

Evaluation of sera of fibromyalgia patients in terms of energy metabolism function and possible alterations in metabolism predisposing to various degenerative/proliferative diseases.

Read the detailed description
  1. Full name of the study: Nuclear Magnetic Resonance Based Metabolomic Profiling in Fibromyalgia Patients
  2. Aim and importance of the study (primary aim, secondary aims, if any): Determination and quantitation of metabolites and enzyme activities by NMR in fibromyalgia patients, changes in citrate, isocitrate, alpha ketoglutarate, alpha ketoglutarate, succinyl CoA, fumarate, malate, glutamate, G-6 PD, phosphogluconate, glyceraldehyde 3 P and oxaloacetate values, especially in energy metabolism in these patients and evaluation of their clinical usefulness will be investigated.
  3. Expected benefits and risks of the research: Fibromyalgia is defined as a chronic syndrome of unknown cause characterized by widespread body pain, fatigue, sleep disturbance, impaired cognitive functioning and anxiety, and possible causes include genetic, neurological, psychological, sleep-related and immunological factors. The disease is 6-9 times more common in women. The diagnosis of fibromyalgia, which has been defined as a true syndrome since the publication of the 1990 classification criteria of the American College of Rheumatology (ACR), is difficult due to the subjectivity of the symptoms, the fact that the evaluation is based on patient reports and the lack of objective diagnostic tests to confirm the diagnosis. The diagnostic criteria for fibromyalgia, which was first described in the 19th century and is the most common rheumatic disease after osteoarthritis, are in constant change. In addition to the difficulty in the diagnosis of the disease, the physiopathology is not fully understood and a specific target for treatment has not been determined. The number of metabolomic studies in serum and urine analyses of patients with fibromyalgia is limited and in order to fill this gap, we will use Bruker 500 MHertz NMR device with an experienced team to examine metabolite determination and quantitation, enzyme activities and especially energy metabolism in Fibromyalgia patients. Thus, it will be investigated whether there is a predisposition to degenerative or proliferative diseases due to acceleration or decrease in energy metabolism in Fibromyalgia patients. According to our literature review, there are no studies investigating both enzymes and metabolites together in fibromyalgia patients. In the published work of researchers, NMR is often used for structure analysis. Quantitative NMR (qNMR), on the other hand, is under development to expand the range of metabolites it can detect in body fluids (to capture low concentrations of substances). qNMR started with very old studies and sub-techniques are being optimized to provide high sensitivity. With the developing technology, this spectrum will expand and in the future, hundreds of metabolites can be determined using a single reference. Although NMR equipment is available in a limited number of universities in our country, we have determined that there is no group working for quantitative analysis as a result of our research. We aim to put our theoretical knowledge into practice with the experience and knowledge of the faculty members of Bezmi Alem Vakıf University Faculty of Medicine within our project. As a starting point for our qNMR studies, we chose fibromyalgia disease, where the number of daily samples reaching our hospital is quite high. In addition, we found that clinical studies on the subject are quite limited. In this sense, the investigators is unique in that it will provide a holistic metabolic profiling in fibromyalgia patients and provide data on adults. The most important problem with the NMR technique is the high costs during the installation of the device, then with low operating costs, the desired analyzes can be performed easily and at low cost in the presence of reference materials and software required for data analysis. We aim to perform quantification of metabolites in body fluids on the NMR device, which has already been installed and is currently in operation at Bezmi Alem Vakıf University. As a starting point, we chose fibromyalgia disease, for which quantitative NMR analysis is very rare in the literature. In terms of sample preparation/analysis procedure for quantitative NMR analyses, it is planned to study serum and urine, which are the first standardized body fluid samples, and samples belonging to the patient population and healthy volunteers. According to the peaks obtained in the NMR spectrum, metabolite identification will be made and quantitation of these metabolites will be performed with the software to be provided for the study.
  4. Type, scope and design of the planned study: In this prospective two-group study, metabolite identification will be performed according to the peaks obtained in the NMR spectrum in 50 patients with clinically diagnosed fibromyalgia and 50 healthy volunteers and it is aimed to perform the quantitation of these metabolites with the software to be provided for the study.
  5. Number of patients and volunteers to be included in the study, their qualifications and rationale for selection: The investigators will be conducted between January 1, 2024 and December 1, 2024 with 50 patients with a diagnosis of fibromyalgia between the ages of 18-65 who meet the inclusion and exclusion criteria of the investigatorsand 50 healthy volunteers. The prior power analysis of the study was performed using the "G. Power-3.1.9.2" program. Means in calculations: Wilcoxon singed-rank test (one sample case) effect size 0.50, alpha 0.05, power 0.90, number of groups 1, number of measures:2, total sample was calculated as 38. A total of 38 patients were planned to be included in the study
  6. Parameters to be analyzed: Measurement of citrate, isocitrate, alpha ketoglutarate, succinyl CoA, fumarate, malate, glutamate, G-6 PD, phosphogluconate, glyceraldehyde 3 P and oxaloacetate levels by NMR technique
  7. Where and by whom the parameters will be checked: The study will be conducted by Specialist Dr. Hatice Kübra Aşık in the outpatient clinic of the Physical Medicine and Rehabilitation Clinic of Private Beykent Hospital. Dr. Hatice Kübra Aşık and biochemical tests will be performed by Prof. Dr. Yıldız Atamer at the Biochemistry Department of Private Beykent Hospital.
  8. Which of the parameters to be used in the study are routine for that disease group and which are specific to the study: Measurement of citrate, isocitrate, alpha ketoglutarate, succinyl CoA, fumarate, malate, glutamate, G-6 PD, phosphogluconate, glyceraldehyde 3 P and oxaloacetate levels by NMR technique not routine for this disease but will be studied in this group for scientific research purposes
  9. Projected duration of work, start and end dates: March 1, 2024 - December 1, 2024
  10. Inclusion, exclusion and withdrawal criteria: Inclusion criteria: Female patients aged 18-65 years Patients with clinical complaints of fibromyalgia (widespread pain, weakness, fatigue, sleep problems, anxiety, restriction of movement, etc.) among the patients applying to the outpatient clinic Exclusion criteria: Viral or bacterial infections, Systemic diseases (diabetes mellitus, hypertension, chronic renal failure, hypo-hyperthyroidism) Patients taking antidepressants or medication, Patients with abnormal laboratory results (erythrocyte sedimentation rate, biochemical or serologic parameters, and thyroid function tests), Smokers and alcohol users, Patients with rheumatic arthritis and systemic lupus erythematosus were excluded. Those who received treatment for tumor
  11. Study termination criteria: The study is planned to be terminated after the completion of the 50 patients and 50 healthy volunteers required for the study.
  12. In the evaluation of the data to be obtained as a result of the research statistical methods to be used:

IBM SPSS (Statistical Package for the Social Sciences) Statistics for Windows, Version 25.0. Armonk, NY: IBM Corp. will be used. In the descriptive statistics of the data, mean and standard deviation values will be used in parametric tests; median values, minimum and maximum values will be used in nonparametric tests.

The distribution of variables will be checked by Kolmogorov-Smirnov test. Paired t test will be used for repeated measurements with normal distribution, while Wilcoxon test will be used for non-normally distributed data. Results will be evaluated at 95% confidence interval and p<0.05 is defined as statistical significance.

  1. Malatji BG, Meyer H, Mason S, et al. NMR metabolomics studies of selected patients and controls based on a diagnostic biomarker profile for fibromyalgia syndrome. BMC Neurology (2017), 17:88
  2. Hsu W-H, Lee C-H, Chao Y-M, et al. ASIC3-dependent metabolomic profiling of serum and urine in fibromyalgia mouse model Scientific Reports, (2019), 9:12123.
  3. Clos-Garcia M, Andrés-Marin N, Fernández-Eulate G, et al. Gut microbiome and serum metabolome analyses identify molecular biomarkers and altered glutamate metabolism in fibromyalgia. EBioMedicine (2019), 46:499-511.
  4. Hackshaw KV, Aykas DP, Sigurdson GT, et al. Metabolic fingerprinting for the diagnosis of fibromyalgia and other rheumatologic disorders. J. Biol. Chem. (2019), 294(7):2555-2568.
  5. Hsu W-H, Han D-S, Ku W-C, et.al. Metabolomic and proteomic characterization of sng and pain phenotypes in fibromyalgia. Eur J Pain, (2022), 26:445-462.
  6. Victoria Menzies, Angela Starkweather, Yingwei Yao, et al. Metabolomic Differences in Women With and Without Fibromyalgia. Clin Transl Sci (2020) 13, 67-77.
  7. Bal SH, Budak F. Overview of Genomics, Proteomics Concepts and Application Areal Journal of Uludag University Faculty of Medicine, 39 (1)65-69, 2013.
  8. Başaran E, Aras S, Cansaran-Duman D. General Outlook and Applications of Genomics, Proteomics and Metabolomics.Turkish Journal of Hygiene and Experimental Biology 2010; 67 (2): 85-96.
  9. Dogan HO. Untargeted Metabolomics Analysis. Sivas Biochemistry Days, November 2-5, 2016.
  10. Marques AP, Santo ASE, Berssaneti AA, Matsutani LA, Yuan SLK. Prevalence of fibromyalgia: literature review update. Rev Bras Reumatol. 2017;57(4):356-363.
  11. Macfarlane GJ, Kronisch C, Dean LE, Atzeni F, Häuser W, Flub E, et al. EULAR revised recommendations for the management of fibromyalgia. Ann Rheum Dis. 2017;76(2):318-328.
Keywords
fibromyalgia, metabolomics profiling
Medical subject headings
Fibromyalgia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06725199
Study groupRoleWhat they receive
Healthy groupBlood and urine samples taken from completely healthy individuals will be examined.
Fibromyalgia groupBlood and urine samples taken from individuals diagnosed with fibromyalgia will be examined

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Metabolomic Profiling

    Biochemical enzymes will be measured by NMR techniques.

    Measured: September 2024- February 2025

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Dec 2024
  2. Study start1 Sep 2024
  3. Primary completion1 Dec 2024 (estimated)
  4. Study completionFeb 2025 (estimated)

Resources

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
Other
Enrolment
100 participants (estimated)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT06725199
Sponsor's protocol ID
E-80929729-000-212940150
Status last verified
Dec 2024
First submitted
4 Dec 2024
Last updated
10 Dec 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: In this prospective two-group study, metabolite identification will be performed according to the peaks obtained in the NMR spectrum in 50 patients with clinically diagnosed fibromyalgia and 50 healthy volunteers and it is aimed to perform the quantitation of these metabolites with the software to be provided for the study. Measurement of citrate, isocitrate, alpha ketoglutarate, succinyl CoA, fumarate, malate, glutamate, G-6 PD, phosphogluconate, glyceraldehyde 3 P and oxaloacetate levels by NMR technique. Measurement of citrate, isocitrate, alpha ketoglutarate, succinyl CoA, fumarate, malate, glutamate, G-6 PD, phosphogluconate, glyceraldehyde 3 P and oxaloacetate levels by NMR technique not routine for this disease but will be studied in this group for scientific research purposes

Publications

  • Malatji BG, Meyer H, Mason S, Engelke UFH, Wevers RA, van Reenen M, Reinecke CJ. A diagnostic biomarker profile for fibromyalgia syndrome based on an NMR metabolomics study of selected patients and controls. BMC Neurol. 2017 May 11;17(1):88. doi: 10.1186/s12883-017-0863-9.

    PubMed 28490352

Questions about this trial

What is this clinical trial studying?

An observational study of Patients with Clinical Complaints of Fibromyalgia Among the Patients Applying to the Outpatient Clinic and Fibromyalgia Syndrome, run by hatice kübra aşık at 1 site in Turkey (Türkiye).

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 1 inclusion and 2 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: enrolling by invitation, as of the sponsor's last update on 10 Dec 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 Turkey (Türkiye). 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?

This study is still under way. Results are not available in the source record yet.

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?

Metabolomic Profiling (time frame: September 2024- February 2025). 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 NCT06725199, which also lists 1 linked publication.

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 10 Dec 2024.

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