Skip to content

Serum Trace Element Levels in Some Gynecological Diseases

Serum Trace Element Profiles in Women With Endometriosis, Ovarian and Endometrial Cancer: An ICP-MS-Based Comparative Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07210918
Enrollment
40
Registered
2025-10-07
Start date
2025-04-24
Completion date
2025-09-29
Last updated
2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometriosis, Endometrial Cancer, Over Cancer, Healthy Control

Keywords

trace elements, endometriosis, endometrial cancer, overian cancer

Brief summary

The aim of this clinical study is to measure the levels of various trace elements in the blood serum of women with various gynecological diseases and to compare them with healthy controls. The main questions it aims to answer are: * Do trace element levels increase or decrease in endometriosis? * Do trace element levels increase or decrease in ovarian cancer patients? * Do trace element levels increase or decrease in endometrial cancer patients? Participants: Each member of the study group will visit the clinic only once and donate 5 ml of blood.

Detailed description

However, the serum trace elements profiles of individuals with endometriosis, ovarian cancer (OC), and endometrial cancer (EC) are not fully known. The purpose of this study is to examine the levels of trace element profiles in the blood serum of healthy people and individuals with gynecological disorders. The study group comprised of 40 women divided into four groups (n=10 each); endometriosis, endometrial cancer and ovarian cancer, and control group who were obstetrically and demographically similar. Inductively coupled plasma-mass spectrometry (ICP-MS) was used to assess serum trace element levels of lead, beryllium, vanadium, chromium, manganese, iron, cobalt, nickel, arsenic, selenium, molybdenum, cadmium, antimony, and phosphorus

Interventions

DIAGNOSTIC_TESTBlood Product

5 mL of blood was collected from the right arms of all individuals in 4 different groups. Their serum was obtained.

Sponsors

Cumhuriyet University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

We have four groups in the study. Blood will be drawn from each group only once. No other interventions will be performed.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Not having received chemotherapy, radiotherapy or immunotherapy in the last three months * For the endometriosis group: histopathologically or laparoscopically confirmed endometriosis * For the ovarian cancer group: histopathologically confirmed epithelial ovarian cancer * For the endometrial cancer group: histopathologically confirmed endometrial adenocarcinoma * For the control group: healthy individuals who underwent surgery for benign gynecological causes (e.g., myoma, benign cyst) and who were not diagnosed with malignancy/endometriosis

Exclusion criteria

* Chronic systemic diseases (e.g., chronic renal failure, liver disease, severe cardiac disease) * Diseases that may affect metabolism or trace element levels (e.g., Wilson's disease, hemochromatosis) * Use of dietary supplements containing minerals or trace elements within the past 6 months * Environmental or occupational heavy metal exposure (e.g., mining, metallurgy, battery industry workers) * Pregnancy or breastfeeding * History of acute infection or inflammatory disease * History of recurrent surgery or advanced metastatic cancer (as this may alter serum parameters) * Psychiatric or cognitive disorders that preclude participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Serum beryllium (Be) measurment3 monthsMeasured beryllium (Be) levels in the serum samples of study group by ICP-MS baseline.
Serum phosphorus (P) measurment3 monthsPhosphorus levels (ppb) in the serum samples of study group by ICP-MS baseline.
Serum vanadium (V) mesurment3 monthsMeasured vanadium (V) levels (ppb) in the serum samples of study group by ICP-MS baseline.
Serum chromium (Cr) measurment3 monthsMeasured chromium (Cr) levels in the serum samples of study group by ICP-MS baseline.
Serum manganese (Mn) measurment3 monthsMeasured manganese (Mn) levels in the serum samples of study group by ICP-MS baseline.
Serum iron (Fe) measurment3 monthsMeasured iron (Fe) levels in the serum samples of study group by ICP-MS baseline.
Serum cobalt (Co) measurment3 monthsMeasured cobalt (Co) levels in the serum samples of study group by ICP-MS baseline.
Serum nickel (Ni) measurment3 monthsMeasured nickel (Ni) levels in the serum samples of study group by ICP-MS baseline.
Serum arsenic (As) measurment3 monthsMeasured arsenic (As) levels in the serum samples of study group by ICP-MS baseline.
Serum selenium (Se) measurment3 monthsMeasured selenium (Se) levels in the serum samples of study group by ICP-MS baseline.
Serum molybdenum (Mo) measurment3 monthsMeasured molybdenum (Mo) levels in the serum samples of study group by ICP-MS baseline.
Serum cadmium (Cd) measurment3 monthsMeasured cadmium (Cd) levels in the serum samples of study group by ICP-MS baseline.
Serum antimony (Sb) measurment3 monthsMeasured antimony (Sb) levels in the serum samples of study group by ICP-MS baseline.
Serum lead (Pb) measurment3 monthsMeasured lead (Pb) levels in the serum samples of study group by ICP-MS baseline.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026