CClinicalTrials.gg
WithdrawnNCT03155828Updated Aug 3, 2018

Using CPAP to Improve Menstruation in Women With Polycystic Ovarian Syndrome and Obstructive Sleep Apnea

An observational study in Sleep Apnea, Obstructive, Anovulation and Polycystic Ovarian Syndrome, sponsored by University of Louisville. Withdrawn at 1 site in United States. Open to female participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2018-08-03.

Sponsored by University of Louisville · Observational

Why this study was withdrawn
Lack of enrollment
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
18 Years to 35 Years
Sex
Female
01

Study summary

The purpose of this study is to determine if treatment of obstructive sleep apnea (OSA) with continuous positive airway pressure in women with both OSA and polycystic ovarian syndrome will improve the regularity of the women's menstrual cycles.

Read the detailed description

Women seeking fertility treatment at the University of Louisville will be screened for polycystic ovarian syndrome (PCOS) based on history and then blood work if history suggests PCOS. After establishing a diagnosis of PCOS based on the National Institute of Health criteria, they will be screened for impaired glucose tolerance, Class III obesity, and obstructive sleep apnea [using the Epworth Sleepiness Scale (ESS) as the initial screen]. For those women that screen positive on the ESS, they will be referred to the University of Louisville Physicians Sleep Center for a formal sleep study. Only patients with PCOS, severe obstructive sleep apnea, impaired glucose tolerance, and Class III obesity will qualify for enrollment in the study. Once enrolled, patients will be encouraged to use continuous positive airway pressure (CPAP, standard of care for treatment of obstructive sleep apnea) for at least six months. During those six months, patients will be asked to track their menstrual cycles and whether they took progesterone to induce a withdrawal bleed during that time period. The use of ovulation predictor kits to help determine ovulation status will be encouraged, but not required for the study.

During initial evaluation, patients seeking fertility care having a clinical presentation concerning for PCOS have their blood drawn for evaluation of thyroid stimulating hormone, free and total testosterone, antimullerian hormone, and 2 hour glucose tolerance test. At the conclusion of six months of CPAP therapy, patients will be asked to repeat the above blood tests for comparison to baseline values.

Women can continue to attempt pregnancy during the study time period if they desire.

02

Conditions studied

  • Sleep Apnea, Obstructive
  • Anovulation
  • Polycystic Ovarian Syndrome

Keywords

  • PCOS, OSA, CPAP
03

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Women seeking fertility treatment at the University of Louisville Reproductive Endocrinology and Infertility Center who have diagnosed polycystic ovarian syndrome, glucose intolerance, obesity, and obstructive sleep apnea.

Inclusion criteria

  • Age 18-35
  • English speakers
  • Polycystic ovarian syndrome by NIH criteria
  • Abnormal 2 hour glucose tolerance test
  • Body mass index >/= 40 kg/m2
  • Severe obstructive sleep apnea diagnosed with either a home or in-house sleep study

Exclusion criteria

Exclusion Criteria:

  • Age \<18 or >35
  • Non English speakers
  • No diagnosis of PCOS
  • Normal glucose tolerance test
  • No diagnosis of obstructive sleep apnea
  • Body mass index \< 40 kg/m2
  • Using any form of hormonal contraception
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)
Patient registry
No

Interventions

  • DeviceCPAP

    Women with diagnosed obstructive sleep apnea will be treated using continuous positive airway pressure as per standard of care.

05

What researchers measure

Primary outcomes

  1. Menstrual Cyclicity

    Resumption of regular cycles as evaluated either by paper menstrual calendar or use of a menstrual cycle application on smart phone or tablet.

    Time frame: 6 months

Secondary outcomes

  1. Ovulation

    Resumption of ovulatory cycles as evaluated by positive ovulation predictor kits.

    Time frame: 6 months

06

Study locations

1 site
  • University of Louisville Fertility Center
    Louisville, Kentucky 40205, United States
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03155828
Lead sponsor
University of Louisville
Responsible party
Kelly Pagidas (Professor, Obstetrics and Gynecology and Women's Health, University of Louisville) — Principal investigator
First posted
May 16, 2017
Start date
Jul 2016
Primary completion
Aug 1, 2018
Completion
Aug 1, 2018
Last update
Aug 3, 2018

Study contacts

Kelly Pagidas, MD
principal investigator · University of Louisville

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Aug 2018. You cannot join it, but the record below documents what was studied.

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