Status:
UNKNOWN
Investigation of ADA Enzyme Deficiency
Lead Sponsor:
TRPHARM
Conditions:
Adenosine Deaminase Deficiency
Eligibility:
All Genders
Up to 40 years
Brief Summary
This observational study was designed as a prospective epidemiological screening study. Patients who applied to the centers participating in the study and were found to be lymphopenic in at least one ...
Detailed Description
Primary immune deficiencies present with signs and symptoms concerning the various disciplines of medicine when compared to other communities in our country on a more frequent basis and are determined...
Eligibility Criteria
Inclusion
- Signing of the written informed consent form by the patient and/or his legal representative,
- The presence of lymphopenia as a result of at least one hemogram of the patient,
- The number of lymphocytes should be below 3000/mm3 for the first 0-12 months
- The number of lymphocytes dec below 1500/mm3 for the first 13 months- ≤ 40 years
- The patient should be 0- ≤ 40 years of age
Exclusion
- The patient was diagnosed with ADA enzyme deficiency before being included in the study,
- The patient has participated in an interventional clinical trial within the last 30 days,
- Failure of the patient himself and/or his legal representative to give their consent to participate in the study,
- According to the researcher's opinion, the patient will not be able to properly fulfill the study requirements,
- Pregnancy and/or lactation period
- The fact that the volunteer participating in the study received an erythrocyte suspension or a complete blood transfusion within the last 3 months.
Key Trial Info
Start Date :
October 10 2019
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
October 10 2022
Estimated Enrollment :
800 Patients enrolled
Trial Details
Trial ID
NCT05300334
Start Date
October 10 2019
End Date
October 10 2022
Last Update
March 29 2022
Active Locations (1)
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1
Ankara Üniversitesi Tıp Fakültesi
Ankara, Mamak, Turkey (Türkiye)