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Daytime Profile of Salivary Progesterone

P

Peter Humaidan

Status

Completed

Conditions

Infertility, Female

Treatments

Diagnostic Test: Progesterone analysis in saliva

Study type

Interventional

Funder types

Other

Identifiers

NCT03725904
Saliva1

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

IVF/FET
Experimental group
Treatment:
Diagnostic Test: Progesterone analysis in saliva

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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