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Clinical Trials/NCT05862805
NCT05862805RecruitingPhase 1

The Role of Plasminogen Activator Inhibitor-1 (PAI-1), Tissue Plasminogen Activator (tPA), Tissue Factor Pathway Inhibitor (TFPI), and Endometrial Endothelial Cells in Uterine Hemostasis in Humans

Oregon Health and Science University1 site in 1 country70 target enrollmentStarted: July 12, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 1
Status
Recruiting
Enrollment
70
Locations
1
Primary Endpoint
Total number of mRNA copies from HEEC culture of tPA

Study Overview

Brief Summary

The purpose of the study is to learn more about the role of blood clotting factor proteins and cells in menstrual (period) bleeding. The investigators are hoping to identify differences in these proteins and cells in the menstrual blood of individuals with heavy periods compared to menstruating individuals who do not have heavy periods.

Detailed Description

The purpose of this study is to learn if human endometrial endothelial cells (HEECs) regulate human uterine hemostasis through the up and down-regulation of pro- and anti-coagulant factors in menstrual blood including PAI-1, factor XI (FXI)-PAI-1 complex, tPA, and TFPI.

This study will enroll participants with heavy menstrual bleeding (HMB) and participants without HMB. Coagulation factors will be measured in menstrual blood and mRNA for these factors will be quantified from cultured HEECS from endometrial biopsies and compared between groups.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Regularly menstruating participants between 18-45 years of age

Exclusion Criteria

  • •Pregnancy within 3 months of enrollment
  • •Lactating at the time of enrollment
  • •Hormonal contraceptive use or use of the copper intrauterine device (IUD)
  • •Antifibrinolytic use
  • •Inherited or acquired bleeding disorder or anticoagulant use
  • •Known structural cause of HMB
  • •Inability to complete PBACs
  • •Unwilling to refrain from sexual intercourse for the two weeks prior to endometrial biopsy

Arms & Interventions

Heavy Menstrual Bleeding

Active Comparator

Participants with heavy menstrual bleeding will provide daily samples of menstrual blood for a single cycle and undergo a single endometrial biopsy for HEEC culture.

Intervention: Sample Collection and Endometrial Biopsy (Procedure)

Regular Mensural Bleeding

Active Comparator

Participants with normal menstrual bleeding will provide daily samples of menstrual blood for a single cycle and undergo a single endometrial biopsy for HEEC culture.

Intervention: Sample Collection and Endometrial Biopsy (Procedure)

Outcomes

Primary Outcomes

Total number of mRNA copies from HEEC culture of tPA

Time Frame: Enrollment to 60 days

The total number of mRNA copies of tPA in HEEC cultures from enrollment to 60 days.

Total number of mRNA copies from HEEC culture of PAI-1

Time Frame: Enrollment to 60 days

The total number of mRNA copies of PAI-1 in HEEC cultures from enrollment to 60 days.

Total number of mRNA copies from HEEC culture of TFPI

Time Frame: Enrollment to 60 days

The total number of mRNA copies of TFPI in HEEC cultures from enrollment to 60 days.

Change in the numerical score of Pictorial Blood Loss Assessment

Time Frame: Enrollment to 60 days

The change in the Pictorial Blood Loss Assessment Charts (PBACs) from baseline to 60 days. Participants will be asked to tally the number of pads and tampons, the level of saturation of menstrual blood on the pads or tampons, and the number of clots. Scores greater than 100 are considered diagnostic of heavy menstrual bleeding.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Bannowb

Principal Investigator

Oregon Health and Science University

Study Sites (1)

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