Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 3:37 PM
Ignite Modification Date:
2025-12-24 @ 3:37 PM
NCT ID:
NCT07083492
Brief Summary:
Validation of non-invasive measurement of zinc protoporphyrin for detection of iron deficiency in pregnancy.
In addition, the impact of iron deficiency on the incidence of postpartum depression, restless legs syndrome, obstetric complications and quality of life will be examined.
Detailed Description:
Study Title Point-of-care transcutaneous longitudinal non-invasive detection of iron deficiency in obstetrics (PICCOLINO Trial)
\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ Brief Summary Iron deficiency is a common condition during pregnancy and is associated with maternal fatigue, increased need for blood transfusion during delivery, and adverse neonatal outcomes. However, current screening practices are inconsistent and often rely on imprecise laboratory parameters like hemoglobin and ferritin. The PICCOLINO trial is a prospective, longitudinal observational study investigating the feasibility and diagnostic value of a novel non-invasive fluorescence-based device to measure zinc protoporphyrin (ZnPP) at the lower lip as a screening tool for iron deficiency in pregnant women.
This study compares non-invasive ZnPP measurements with conventional blood-based markers for iron deficiency and anemia at five time points: once in each trimester, at the time of delivery, and approximately 2-3 months postpartum. The study further examines correlations between iron status and maternal well-being, postpartum depression, restless legs syndrome (RLS), and pregnancy complications.
\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ Detailed Description The study enrolls up to 500 pregnant women, aiming to start inclusion as early as the first trimester. In each participant, ZnPP will be measured non-invasively at the lower lip using an optical sensor. Concurrently, venous blood samples will be drawn (where possible during routine care) to assess standard hematological and iron-related parameters (Hb, MCV, MCH, ferritin, transferrin saturation, Ret-Hb, RDW, and serum zinc).
Validated questionnaires will be used to assess:
* General health-related quality of life (SF-12)
* Postpartum depression (EPDS)
* Restless legs syndrome (IRLS)
* Nutrition and supplement intake
* Birth experience (SCIB) The primary aim is to validate the diagnostic performance of non-invasive ZnPP measurements as a screening tool for iron deficiency in pregnancy. Receiver operating characteristic (ROC) analysis will be conducted to compare non-invasive measurements with expert opinion diagnoses and blood-based markers. Secondary outcomes include the relationship between iron deficiency and maternal fatigue, mood disorders, pregnancy outcomes, and neonatal parameters.
Study Design
* Type: Observational (Longitudinal Cohort)
* Duration per participant: Up to 12 months
* Estimated Enrollment: 500 participants
* Timepoints: 1st, 2nd, 3rd trimester, peripartum, and 60-90 days postpartum
* Location: University Hospital Würzburg, Germany
Eligibility Criteria
Inclusion Criteria:
* Pregnant women aged ≥18 years
* Any gestational age or shortly postpartum
* Written informed consent
Exclusion Criteria:
* Previous participation in the study
* Decline of blood sampling for study purposes
* Inability to provide informed consent
Outcome Measures
Primary Outcome:
• Diagnostic performance (ROC/AUC) of non-invasive ZnPP in detecting iron deficiency
Secondary Outcomes:
* Correlation of iron status with quality of life, postpartum depression, and RLS
* Relationship between iron deficiency and pregnancy/neonatal complications
Study:
NCT07083492
Study Brief:
Protocol Section:
NCT07083492