Detecting Abnormal Fetal Karyotype by the Electronic Nose Clinical Trial
Official title:
Examining the Ability of Electronic Nose in Detecting Fetal Chromosomal Disorders
Verified date | September 2015 |
Source | Rambam Health Care Campus |
Contact | n/a |
Is FDA regulated | No |
Health authority | Israel: Ministry of Health |
Study type | Observational |
"electronic nose"- the tiny sensors, will smell and detect the changes in the sample of abnormal fetal karyotype, and fluid that will be confirmed by amniocentesis.
Status | Not yet recruiting |
Enrollment | 500 |
Est. completion date | August 2017 |
Est. primary completion date | August 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 16 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Pregnant women candidates for amniocentesis - 17-33 gestational weeks Exclusion Criteria: - women that refuse to participate in the research - women older than 45 or less than 16 |
Observational Model: Case Control, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
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Rambam Health Care Campus |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Examining the ability of the electronic nose in detecting abnormal fetal karyotype | the electronic nose can detect various diseases Including cancer and asthma on basis of evaporable substances. The device simulates the human nose ", which includes an array of tiny sensors connected to nanometric sizes electronic calculating unit. 30 cc of amniotic fluid are part of routine tests and the rest of the amount (3 ml) is intended for research, this sample will be saved in cooling (-20) and subsequently transferred to the Technion, for examination by electronic sensors. The amount of amniotic fluid designed for research is a minimal amount and will not hurt the fetus. At the end of the study following the data processing, we will be able to appreciate the effectiveness of the electronic nose in diagnosing fetal chromosomal disorders. |
3 years | No |