Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06802861 · ClinicalTrials.gov registry record

Relationship Between Aspirin Metabolism and Markers of Metabolic Dysfunction Among Pregnant Persons at Risk of Pre-eclampsia

A clinical trial of Pregnancy and Preeclampsia, sponsored by University of Tennessee Graduate School of Medicine.

Recruiting
Registry status
50
Enrollment target
1
Study location

NCT06802861: Recruiting study of Pregnancy and Preeclampsia, sponsored by University of Tennessee Graduate School of Medicine.

NCT06802861 is a study of Pregnancy and Preeclampsia that is actively recruiting participants, run by University of Tennessee Graduate School of Medicine. The registered enrollment target is 50 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06802861, a study of Pregnancy and Preeclampsia, is actively recruiting participants, sponsored by University of Tennessee Graduate School of Medicine.

RECRUITING
Registry status
50 participants
Enrollment target
1
Study location

Study Summary

This study's primary purpose is to determine the relationship between aspirin metabolism and markers of metabolic dysfunction among patients at risk for preeclampsia.

Primary Outcome

Hexadecadienoate (long chain poly unsaturated fatty acid metabolite obtained from metabolomics assay) (z score)

Study Locations (1)

Tennessee

  • University of Tennessee Medical Center - Knoxville

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2025-01-01
Est. Completion 2028-12-31

What NCT06802861 shows while recruiting

NCT06802861 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (94% lower).

The record links to 9 conditions, with Pregnancy appearing as the primary indexed condition, and to 0 interventions.

NCT06802861 reports a single indexed study location in Tennessee.

Frequently Asked Questions

What is clinical trial NCT06802861 about?

NCT06802861 is a clinical study titled "Relationship Between Aspirin Metabolism and Markers of Metabolic Dysfunction Among Pregnant Persons at Risk of Pre-eclampsia". This study's primary purpose is to determine the relationship between aspirin metabolism and markers of metabolic dysfunction among patients at risk for preeclampsia.

What is the current status of trial NCT06802861?

This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2025-01-01. Estimated completion is 2028-12-31.

What conditions does trial NCT06802861 study?

This clinical trial studies the following conditions: Pregnancy, Preeclampsia, Gestational Diabetes, Pregnancy Complications, Obesity and Obesity-related Medical Conditions.

Who is sponsoring clinical trial NCT06802861?

This trial is sponsored by University of Tennessee Graduate School of Medicine, which has 20 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06802861 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pregnancy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06802861's enrollment target sits among peer trials

50 152nd of 191 higher than 34 of 191 other Pregnancy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pregnancy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00200889 · 50 participants · Early Phase 1

    Mapping Auricular Vagus Nerve Circuitry

  • NCT00409435 · 50 participants · Phase 2

    A Study of Pyridostigmine in Postural Tachycardia Syndrome

  • NCT01202305 · 50 participants

    The Use of Lymph Node Biopsies to Support HIV Pathogenesis Studies

  • NCT01225913 · 50 participants · Phase 4

    Mechanism(s) of Airflow Limitation During Exacerbation of Asthma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06802861, the US trial registry maintained by the National Library of Medicine. NCT06802861 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.