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

NCT06518174 · ClinicalTrials.gov registry record · NA

A Novel Imaging Modality to Evaluate Radiation-Induced Uterine Injury

A NA study of Uterine Injury, sponsored by University of Colorado, Denver.

Recruiting
Registry status
NA
Development phase
22
Enrollment target
1
Study location

NCT06518174: Recruiting NA study of Uterine Injury, sponsored by University of Colorado, Denver.

NCT06518174 is a NA study of Uterine Injury that is actively recruiting participants, run by University of Colorado, Denver. The registered enrollment target is 22 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% 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

NCT06518174, a NA study of Uterine Injury, is actively recruiting participants, sponsored by University of Colorado, Denver.

RECRUITING
Registry status
NA
Development phase
22 participants
Enrollment target
1
Study location

Study Summary

The goal of this pilot study is to assess the ability of a new imaging modality, shear-wave-elastography (SWE) and magnetic resonance imaging (MRI) to identify radiation-induced uterine injury (RIUI). The investigator will recruit female patients treated before 40 years with pelvic radiation (PRT) at least 12 months prior to study initiation.

Primary Outcome

SWE will be considered feasible if at least 85% (e.g., ≥15/17) of all patients achieve the diagnosability criteria, defined as having at least 1 of 6 locations with IQR/M ≤ 30%. The IQR/M and the number of patients who achieved diagnosability will be descriptively characterized.

Conditions Studied

Interventions

  • DIAGNOSTIC_TEST MRI, SWE, and US evaluation

Study Locations (1)

Colorado

  • University of Colorado - Aurora

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2025-02-25
Est. Completion 2027-03
Phase NA
University of Colorado, Denver

1,283 total trials

What NCT06518174 shows while recruiting

NCT06518174 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Uterine Injury appearing as the primary indexed condition, and to 1 intervention - of which MRI, SWE, and US evaluation is the first listed.

NCT06518174 reports a single indexed study location in Colorado.

Frequently Asked Questions

What is clinical trial NCT06518174 about?

NCT06518174 is a clinical study titled "A Novel Imaging Modality to Evaluate Radiation-Induced Uterine Injury". The goal of this pilot study is to assess the ability of a new imaging modality, shear-wave-elastography (SWE) and magnetic resonance imaging (MRI) to identify radiation-induced uterine injury (RIUI). The investigator will recruit female patients treated before 40 years with pelvic radiation (PRT) a...

What is the current status of trial NCT06518174?

This trial is currently recruiting. It is a NA study. The enrollment target is 22 participants. The study started on 2025-02-25. Estimated completion is 2027-03.

What conditions does trial NCT06518174 study?

This clinical trial studies the following conditions: Uterine Injury.

What interventions are being tested in trial NCT06518174?

The interventions under investigation include: MRI, SWE, and US evaluation (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT06518174?

This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06518174 being conducted?

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

How this trial's enrollment target compares

Where NCT06518174's enrollment target sits among peer trials

22 1756th of 2000 higher than 239 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

  • NCT02508038 · 22 participants · Phase 1

    Alpha/Beta CD19+ Depleted Haploidentical Transplantation + Zometa for Pediatric Hematologic Malignancies and Solid Tumors

  • NCT03099356 · 22 participants · Phase 2

    Cyclophosphamide and Sirolimus for the Treatment of Metastatic, RAI-refractory, Differentiated Thyroid Cancer

  • NCT03676647 · 22 participants

    Diagnostic DNA Methylation Signature in Diagnosing Thyroid Cancer After Fine-Needle Aspiration in Patients With Thyroid Nodules

  • NCT04569591 · 22 participants · NA

    DDAVP for Pituitary Adenoma

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 NCT06518174, the US trial registry maintained by the National Library of Medicine. NCT06518174 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.