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

NCT05100342 · ClinicalTrials.gov registry record

Prospective Validation of a Points Score System Predicting 30-day Survival

A clinical trial of Metastatic Cancer, sponsored by Indiana University.

Recruiting
Registry status
114
Enrollment target
3
Study locations

NCT05100342: Recruiting study of Metastatic Cancer, sponsored by Indiana University.

NCT05100342 is a study of Metastatic Cancer that is actively recruiting participants, run by Indiana University. The registered enrollment target is 114 participants, below the 443-participant average among 109 other Metastatic Cancer trials with a reported enrollment target (74% lower). The trial reports 3 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05100342, a study of Metastatic Cancer, is actively recruiting participants, sponsored by Indiana University.

RECRUITING
Registry status
114 participants
Enrollment target
3
Study locations

Study Summary

This is a one-stage single-arm phase II clinical trial designed to prospectively test the survival prediction tool as developed by Lee et al on patients referred to radiation oncology for palliative treatments. Survival prediction score based on objective data including laboratory values, attendance to emergency room, and primary cancer origin will be assigned to each patient at time of enrollment.

Primary Outcome

The percentage of patients with a score of \>14 who are living at 30 days following enrollment

Conditions Studied

Interventions

  • DIAGNOSTIC_TEST Point score prediction tool for 30-day survival

Study Locations (3)

Indiana

  • IU Health West - Avon
  • IU Health North / Schwarz Cancer Center - Carmel
  • Methodist Hospital - Indianapolis

Trial Details

FieldValue
Enrollment Target 114 participants
Start Date 2022-09-12
Est. Completion 2027-12
Indiana University

890 total trials

What NCT05100342 shows while recruiting

NCT05100342 is an observational study that tracks outcomes without assigning an intervention. The registered 114 participants enrollment target is mid-sized for trials with a published cap, below the 443-participant average among 109 other Metastatic Cancer trials with a reported enrollment target (74% lower).

The record links to 1 condition, with Metastatic Cancer appearing as the primary indexed condition, and to 1 intervention - of which Point score prediction tool for 30-day survival is the first listed.

NCT05100342 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT05100342 about?

NCT05100342 is a clinical study titled "Prospective Validation of a Points Score System Predicting 30-day Survival". This is a one-stage single-arm phase II clinical trial designed to prospectively test the survival prediction tool as developed by Lee et al on patients referred to radiation oncology for palliative treatments. Survival prediction score based on objective data including laboratory values, attendance...

What is the current status of trial NCT05100342?

This trial is currently recruiting. The enrollment target is 114 participants. The study started on 2022-09-12. Estimated completion is 2027-12.

What conditions does trial NCT05100342 study?

This clinical trial studies the following conditions: Metastatic Cancer.

What interventions are being tested in trial NCT05100342?

The interventions under investigation include: Point score prediction tool for 30-day survival (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT05100342?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05100342 being conducted?

This trial has 3 study locations across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Metastatic Cancer

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 NCT05100342's enrollment target sits among peer trials

114 37th of 109 higher than 73 of 109 other Metastatic Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Metastatic Cancer 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

  • NCT04522791 · 114 participants · Phase 2

    Breathing, Relaxation, Attention Training, & Health in Older Adults (BREATHE)

  • NCT04875052 · 114 participants · NA

    Vibration and Post-traumatic Osteoarthritis Risk Following ACL Injury

  • NCT05224089 · 114 participants · Phase 4

    Bilateral TAP and RS Blocks Using Liposomal Bupivacaine/Bupivacaine vs. Regular Bupivacaine in Laparoscopic Colectomy

  • NCT05389332 · 114 participants · NA

    A Mobile Health Intervention Among Hispanics

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 NCT05100342, the US trial registry maintained by the National Library of Medicine. NCT05100342 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.