Non-invasive Imaging Technique for the Study of Lordosis in Pregnant Women and Its Relationship to Birth Outcome
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20-40
SponsorUniversity of Alcala
About this trial
The study consists of collecting measurement data of the rachis in pregnant women and the subsequent outcome of her delivery.
This will make it possible to validate a non-invasive imaging technique through software that can be used to study this anatomical curve proposing a new measurement method for the angle of lordosis.
Finally, with the research data, the investigators will try to find a correlation between these variables (angle of lordosis and delivery outcome.
Eligibility criteria
Qualifiers
pregnant women between 20 and 40 years old with a low-risk pregnancy
Disqualifiers
Pregnant women under 20 years and over 40 years of age or with a significant lumbar pathology or with a very high-risk pregnancy or with IMC >35
Trial design
Treatments tested in this trial
- Arrow Test
- Angle measurement by imaging device
Treatment groups
122 Participants
are divided into 1 treatment groupLocations
1University of Alcalá28871, Alcalá de HenaresMadrid, Spain
Sponsors and collaborators
University of Alcala
Lead sponsor
Hospital Universitario de Fuenlabrada
Collaborator
Source ClinicalTrials.gov