MedPath

Daytime Profile of Salivary Progesterone

Not Applicable
Completed
Conditions
Infertility, Female
Registration Number
NCT03725904
Lead Sponsor
Peter Humaidan
Brief Summary

The aim of this study is to perform a 12-hour profile of free saliva progesterone during the luteal phase after fresh and frozen embryo transfer. If progesterone levels in saliva samples show a constant level during daytime, this non-invasive measurement can be used in future ART patients with insufficient progesterone levels who might benefit from additional exogenous progesterone supplementation.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
20
Inclusion Criteria
  • 18-45 years
  • One or two good quality embryos for transfer on day 5.
  • BMI >18,5 <30 kg/m²
Exclusion Criteria
  • No good quality embryos for transfer
  • Uterine abnormalities
  • One ovary
  • Oocyte donation

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Levels of free progesterone in saliva12 hours
Secondary Outcome Measures
NameTimeMethod
Clinical pregnancy rate8 weeks

Ultrasound detected gestational sack divided with number of embryo transfer

Ongoing pregnancy rate12 weeks

Viable pregnancy after gestational week 12+0

Trial Locations

Locations (1)

Fertility Clinic Regional Hospital Skive

🇩🇰

Skive, Denmark

Fertility Clinic Regional Hospital Skive
🇩🇰Skive, Denmark

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