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

NCT04476589 · ClinicalTrials.gov registry record

Prognostication of Recovery in Early Disorders of Consciousness After COVID-19

A clinical trial of COVID-19 and Coma, sponsored by Massachusetts General Hospital.

Completed
Registry status
12
Enrollment target
1
Study location

NCT04476589: Completed study of COVID-19 and Coma, sponsored by Massachusetts General Hospital.

NCT04476589 is a study of COVID-19 and Coma that has completed, run by Massachusetts General Hospital. The registered enrollment target is 12 participants, below the 38,465-participant average among 298 other COVID-19 trials with a reported enrollment target (100% 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

NCT04476589, a study of COVID-19 and Coma, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
12 participants
Enrollment target
1
Study location

Study Summary

The primary aim of this research proposal is to use multimodal metrics (e.g., clinical data and advanced neuroimaging) in the early (i.e., acute hospitalization) phase of recovery from COVID-19-related disorders of consciousness to predict outcome at 3, 6, and 12 months post-hospitalization. We aim to construct an algorithm that synthesizes the results of these metrics to help predict recovery.

Primary Outcome

Functional outcome measure. Maximum score of 29 represents high disability, minimum score of 0 represents no disability. Higher scores represent higher level of disability.

Interventions

  • DIAGNOSTIC_TEST Functional MRI

Study Locations (1)

Massachusetts

  • Massachusetts General Hospital - Boston

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2020-07-01
Est. Completion 2022-04-07
Massachusetts General Hospital

2,032 total trials

What the finished NCT04476589 record still lists

NCT04476589 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 38,465-participant average among 298 other COVID-19 trials with a reported enrollment target (100% lower).

The record links to 3 conditions, with COVID-19 appearing as the primary indexed condition, and to 1 intervention - of which Functional MRI is the first listed.

NCT04476589 reports a single indexed study location in Massachusetts.

Frequently Asked Questions

What is clinical trial NCT04476589 about?

NCT04476589 is a clinical study titled "Prognostication of Recovery in Early Disorders of Consciousness After COVID-19". The primary aim of this research proposal is to use multimodal metrics (e.g., clinical data and advanced neuroimaging) in the early (i.e., acute hospitalization) phase of recovery from COVID-19-related disorders of consciousness to predict outcome at 3, 6, and 12 months post-hospitalization. We aim ...

What is the current status of trial NCT04476589?

This trial is currently completed. The enrollment target is 12 participants. The study started on 2020-07-01. Estimated completion is 2022-04-07.

What conditions does trial NCT04476589 study?

This clinical trial studies the following conditions: COVID-19, Coma, Consciousness Disorder.

What interventions are being tested in trial NCT04476589?

The interventions under investigation include: Functional MRI (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT04476589?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04476589 being conducted?

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

Similar trials for COVID-19

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 NCT04476589's enrollment target sits among peer trials

12 292nd of 298 higher than 6 of 298 other COVID-19 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other COVID-19 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

  • NCT02602769 · 12 participants

    Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome

  • NCT02605421 · 12 participants · Phase 2

    Myeloablative Consolidation Therapy and Tandem Autologous Stem Cell Rescue in Patients With High-Risk Neuroblastoma

  • NCT02619448 · 12 participants · Early Phase 1

    Concurrent Chemotherapy Plus HFR Radiation Therapy in Inoperable NSCLC

  • NCT03311503 · 12 participants · Phase 1

    Phase I/II Trial of Lentiviral Gene Transfer for SCID-X1 With Low Dose Targeted Busulfan Conditioning

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 NCT04476589, the US trial registry maintained by the National Library of Medicine. NCT04476589 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.