Purpose

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.

Condition

Eligibility

Eligible Ages
Between 18 Years and 45 Years
Eligible Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Born with a uterus - 18-45 years old - With and without endometriosis

Exclusion Criteria

  • Currently pregnant or breastfeeding - Diagnosed cardiovascular disease - BMI over 35 - Nicotine use (e.g., smoking, chewing tobacco, vaping, etc.) - Currently using hormone replacement therapy (or have used within previous 6 months) - Known skin allergies or current rash, skin disease, disorders of pigmentation - Diabetes - Renal disease, renal artery stenosis, renal impairment - Liver disease - Stage II Hypertension (blood pressure >140/>90 mmHg) - Hypotension (blood pressure < 90/60 mmHg) - Raynaud's syndrome - Any current medications which could conceivably alter cardiovascular responses (e.g. antihypertension medication, diuretic, digoxin) - Allergy or hypersensitivity to investigational agents - Immunosuppressed/immunocompromised

Study Design

Phase
Phase 4
Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover Assignment
Primary Purpose
Basic Science
Masking
Single (Participant)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Aspirin
one dose of aspirin
  • Drug: Aspirin
    650 mg aspirin (Acetylsalicylic acid)
Placebo Comparator
Placebo
Placebo pill
  • Other: Placebo
    placebo capsule

Recruiting Locations

Noll Laboratory
University Park, Pennsylvania 16802
Contact:
Lacy Alexander, Ph.D.
814-867-1781
lma191@psu.edu

More Details

NCT ID
NCT05962034
Status
Recruiting
Sponsor
Penn State University

Study Contact

Lacy Alexander, Ph.D.
8148671781
lma191@psu.edu

Detailed Description

Cardiovascular disease (CVD) is the leading cause of death worldwide. Endometriosis is an independent risk factor for CVD that affects an estimated one in ten women in the world. Endometriosis is a gynecologic condition characterized by invasive extrauterine endometriotic lesions, chronic pain, and systemic inflammation. The expression of thromboxane A2 (TxA2), a product of the inflammatory cyclooxygenase pathway, is upregulated in endometriotic lesions. In the vasculature, TxA2 blocks vasodilation, and induces vasoconstriction. TxA2 diffuses across the innermost layer of cells in the blood vessels, the endothelium, to act directly on its receptors in the vascular smooth muscle. It also inhibits endothelial nitric oxide synthase, thereby decreasing nitric oxide (NO)-mediated vasodilation --endothelial dysfunction which is regarded as a critical early event in the development of atherosclerosis and overt cardiovascular disease. Women with endometriosis demonstrate marked endothelial dysfunction compared with healthy controls, but the potential role of TxA2 and its receptors (TP) in this dysfunction have not been investigated. Furthermore, TP play a key role in sensitizing the sensory afferent nerve fibers in pre-clinical models of cardiovascular disease, leading to an exaggerated blood pressure responses to sympathoexcitatory maneuvers including the exercise pressor reflex. The exercise pressor reflex is the reflex increase in blood pressure in response to the mechanical and metabolic stimuli of exercise. The exaggeration of this reflex response is a strong predictor of major adverse cardiovascular events in cardiovascular disease patients. However, the reflex response to sympathoexcitatory maneuvers has not been characterized in women with endometriosis. Furthermore, TxA2 is a key component in the clotting cascade. An increased production of TxA2 in the platelet cells of women with endometriosis indicates altered platelet function. However, platelet activity in women with endometriosis has not been characterized.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.