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NCT05021237 · ClinicalTrials.gov registry record · Phase 2

Personalized Ultra-fractionated Stereotactic Adaptive Radiotherapy for Metastatic Cervical Cancer

A Phase 2 study of Cervical Cancer and Metastasis, sponsored by University of Texas Southwestern Medical Center.

Active
Registry status
Phase 2
Development phase
12
Enrollment target
1
Study location

NCT05021237 is a Phase 2 study of Cervical Cancer and Metastasis that is active but no longer recruiting, run by University of Texas Southwestern Medical Center. The registered enrollment target is 12 participants, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05021237, a Phase 2 study of Cervical Cancer and Metastasis, is active but no longer recruiting, sponsored by University of Texas Southwestern Medical Center.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
12 participants
Enrollment target
1
Study location

Study Summary

To improve overall survival in patients with metastatic cervical cancer by loco-regional therapy with personalized ultra-fractionated radiation

Interventions

  • RADIATION Ultra-fractionated radiation therapy

Study Locations (1)

Texas

  • UT Southwestern Medical Center - Dallas

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2022-02-01
Est. Completion 2028-08
Phase Phase 2

What the Registry Record Tells You About NCT05021237

The ClinicalTrials.gov registry entry for NCT05021237 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 570-participant average among 144 other Cervical Cancer trials with a reported enrollment target (98% lower). The listed sponsor is University of Texas Southwestern Medical Center, which has 837 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Cervical Cancer appearing as the primary indexed condition, and to 1 intervention - of which Ultra-fractionated radiation therapy is the first listed.

NCT05021237 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05021237 about?

NCT05021237 is a clinical study titled "Personalized Ultra-fractionated Stereotactic Adaptive Radiotherapy for Metastatic Cervical Cancer". To improve overall survival in patients with metastatic cervical cancer by loco-regional therapy with personalized ultra-fractionated radiation

What is the current status of trial NCT05021237?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 12 participants. The study started on 2022-02-01. Estimated completion is 2028-08.

What conditions does trial NCT05021237 study?

This clinical trial studies the following conditions: Cervical Cancer, Metastasis, Stage IV Cervical Cancer FIGO 2018, Adenosquamous Carcinoma of Cervix.

What interventions are being tested in trial NCT05021237?

The interventions under investigation include: Ultra-fractionated radiation therapy (RADIATION).

Who is sponsoring clinical trial NCT05021237?

This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05021237 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.