Actively Recruiting

Phase 4
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
NCT05962034

Thromboxane Function in Women With Endometriosis

Led by Penn State University · Updated on 2025-05-04

96

Participants Needed

1

Research Sites

186 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare neurovascular regulation in women with endometriosis and healthy women. The main questions it aims to answer are: * Do women with endometriosis have greater blood pressure and pain responses to a stimulus than healthy women? * Do women with endometriosis have greater platelet activity than healthy women? Participants will take aspirin and/or placebo and will: * perform hand grip exercise and cold pressor tests * undergo iontophoresis and blood draw Researchers will compare women with and without endometriosis to see if there is a difference in neurovascular regulation.

CONDITIONS

Official Title

Thromboxane Function in Women With Endometriosis

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Born with a uterus
  • 18-45 years old
  • Women with and without endometriosis
Not Eligible

You will not qualify if you...

  • Currently pregnant or breastfeeding
  • Diagnosed cardiovascular disease
  • Body mass index over 35
  • Use of nicotine products such as smoking, chewing tobacco, or vaping
  • Current or recent (within 6 months) hormone replacement therapy
  • Known skin allergies, current rash, skin disease, or pigmentation disorders
  • Diabetes
  • Kidney disease, renal artery stenosis, or kidney impairment
  • Liver disease
  • Stage II hypertension (blood pressure over 140/90 mmHg)
  • Low blood pressure (below 90/60 mmHg)
  • Raynaud's syndrome
  • Use of medications that could affect cardiovascular responses (e.g., antihypertensives, diuretics, digoxin)
  • Allergy or sensitivity to investigational agents
  • Immunosuppressed or immunocompromised status

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Noll Laboratory

University Park, Pennsylvania, United States, 16802

Actively Recruiting

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Research Team

L

Lacy Alexander, Ph.D.

CONTACT

S

Sue Slimak, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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