Clinical Trials Directory

Trials / Unknown

UnknownNCT02862496

Bone Health in Hyperemesis Gravidarum

Urine N-telopeptide, Serum Vit D, Parathormone and Calcium Levels in Hyperemesis Gravidarum

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Kayseri Education and Research Hospital · Other Government
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to determine whether maternal bone resorption would be seen in Hyperemesis Gravidarum and could be detected in early period using serum vitamin D levels, serum calcium (Ca) levels, serum parathormone (PTH) levels and urine N- telopeptide levels in the patients with Hyperemesis Gravidarum.

Conditions

Timeline

Start date
2016-06-01
Primary completion
2016-10-01
Completion
2016-10-01
First posted
2016-08-11
Last updated
2016-08-11

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02862496. Inclusion in this directory is not an endorsement.