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Daytime Profile of Salivary Progesterone

NCT03725904 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2020-01-22

No results posted yet for this study

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.

Conditions

  • Infertility, Female

Interventions

DIAGNOSTIC_TEST

Progesterone analysis in saliva

Analysis of salava progesterone

Sponsors & Collaborators

  • Boston IVF

    collaborator OTHER

  • Peter Humaidan

    lead OTHER

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-10-24
Primary Completion
2019-04-03
Completion
2020-01-01

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03725904 on ClinicalTrials.gov