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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01644318
Other study ID # 3848
Secondary ID
Status Active, not recruiting
Phase N/A
First received July 17, 2012
Last updated July 18, 2012

Study information

Verified date July 2012
Source Ankara Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority Turkey: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to measure serum CXCL9 and CXCL11 levels in patients with autoimmune thyroiditis and habitual abortions


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- non-pregnant women with euthyroid autoimmune thyroiditis and a history of first trimester recurrent spontaneous abortions

Exclusion Criteria:

- 1) presence of acute or chronic systemic diseases; 2) other autoimmune diseases; 3) pregnancy and lactation over the previous 6 months; 4) evidence of infectious diseases in the last 3 months; 5) treatment with drugs known to interfere with cytokine release, such as corticosteroids, immunosuppressors, or nonsteroidal antiinflammatory drugs, amiodarone, and lithium; 6) clinical history of hyperthyroidism and/or the presence of anti-TSH receptor antibodies.

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Ankara Education and Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Serum CXCL9 and CXCL11 levels in patients with autoimmune thyroiditis and habitual abortions
See also
  Status Clinical Trial Phase
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Completed NCT00959621 - Low Molecular Weight Heparin and/or Aspirin in Prevention of Habitual Abortion Phase 3
Completed NCT00772122 - Use of G-CSF for the Treatment of Unexplained Recurrent Miscarriage Phase 4
Completed NCT04017754 - Low Plasma Mannose Binding Lectin (p-MBL) Level is a Risk Factor for Recurrent Pregnancy Loss (RPL)
Recruiting NCT04701034 - Intravenous Immunoglobulin and Prednisolone for RPL After ART. Phase 2
Recruiting NCT05169541 - Association Between Plasma Level of Mannose Binding Lectin and Human Reproduction