Skip to main content
Clinical Trials/DRKS00016746
DRKS00016746
Completed
Not Applicable

Helminth infection during pregnancy alters immune responses at the fetomaternal interface - HelmVit_Pilotstudy

Institut für Mikrobiologie, Immunologie und Hygiene, Technische Universität München0 sites102 target enrollmentApril 30, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Haematology and clinical chemistry, Vitamin Status
Sponsor
Institut für Mikrobiologie, Immunologie und Hygiene, Technische Universität München
Enrollment
102
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 30, 2019
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Sponsor
Institut für Mikrobiologie, Immunologie und Hygiene, Technische Universität München

Eligibility Criteria

Inclusion Criteria

  • Presence of written consent
  • \- Age \> 18 years
  • \- feminine
  • \- Persons who are legally competent and mentally able to understand and follow the instructions of the study staff.
  • \- Patient information and written declaration of consent of the test person
  • \- Adequate bone marrow reserve with a peripheral granulocyte count \>1500/µl and platelet count \>40\.000/µl
  • \- No condition after recurrent thrombosis or pulmonary embolism
  • \- no serious abnormalities during the physical examination
  • \- Documentation of known anaphylaxias

Exclusion Criteria

  • \- Presence of the following autoimmune diseases: Anti\-phospholipid, antibody syndrome, Goodpasture syndrome, Sjögren syndrome, rheumatoid arthritis, lupus erythematosus, sarcoidosis, anti\-neutrophilic cytoplasmic antibodies (ANCA syndrome), scleroderma, chronic polychondritis
  • \- The following known immunodepressing diseases: X\-chromosomal A\-?\-Globulinemia, severe combined immunodeficiency (SCID), common variable immunedeficiency (CVID), selective IgA deficiency
  • \- known hepatitis B and/or C, HIV, HSV, CMV, syphilis, toxoplasmosis infection
  • \- other, severe, active infection
  • \- ongoing corticosteroid treatment
  • \- transfusion\-dependent anemia
  • \- any other disease or medical treatment which, in the opinion of the investigator, would militate against participation in the study, e.g. (pre\-)eclampsia, HELLP syndrome
  • \- Persons who have a dependent/labour relationship with the sponsor or investigator.
  • \- known cancers currently or in the past

Outcomes

Primary Outcomes

Not specified

Similar Trials