Sleep in Women With Bilateral Salpingo-Oophorectomy

NCT ID: NCT04565158

Last Updated: 2024-09-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

71 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-12-14

Study Completion Date

2023-11-06

Brief Summary

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The purpose of this research study is the compare objective and subjective sleep characteristics in women who have undergone removal of both ovaries (bilateral salpingo-oophorectomy) before natural menopause compared to women who did not undergo this procedure.

Detailed Description

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Conditions

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Bilateral Salpingo-oophorectomy

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Women with bilateral salpingo-oophorectomy (BSO)

No interventions assigned to this group

Women without bilateral salpingo-oophorectomy (BSO)

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Women who participate in the parent SCORE studies (NCT03821857)

Exclusion Criteria

* Night shift workers will be excluded
Minimum Eligible Age

55 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Naima Covassin

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Naima Covassin, PhD

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

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Mayo Clinic in Rochester

Rochester, Minnesota, United States

Site Status

Countries

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United States

Related Links

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Other Identifiers

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20-005982

Identifier Type: -

Identifier Source: org_study_id

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