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

NCT06475898 · ClinicalTrials.gov registry record

Longitudinal Endpoint Assessment of Disease Burden in HD

A clinical trial of Huntington Disease, sponsored by Huntington Study Group.

Recruiting
Registry status
600
Enrollment target
1
Study location

NCT06475898: Recruiting study of Huntington Disease, sponsored by Huntington Study Group.

NCT06475898 is a study of Huntington Disease that is actively recruiting participants, run by Huntington Study Group. The registered enrollment target is 600 participants, roughly in line with the 618-participant average among 35 other Huntington Disease trials with a reported enrollment target. 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

NCT06475898, a study of Huntington Disease, is actively recruiting participants, sponsored by Huntington Study Group.

RECRUITING
Registry status
600 participants
Enrollment target
1
Study location

Study Summary

LEAD-HD is intended to collect and analyze self-reported health information from individuals with Huntington Disease (HD) or prodromal HD participating in a 24-month longitudinal natural history study using remote technologies.

Primary Outcome

Obtain PRO natural history data in HD.

Conditions Studied

Study Locations (1)

New York

  • Huntington Study Group - Rochester

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2024-06-25
Est. Completion 2026-12
Huntington Study Group

5 total trials

What NCT06475898 shows while recruiting

NCT06475898 is an observational study that tracks outcomes without assigning an intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 618-participant average among 35 other Huntington Disease trials with a reported enrollment target.

The record links to 1 condition, with Huntington Disease appearing as the primary indexed condition, and to 0 interventions.

NCT06475898 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT06475898 about?

NCT06475898 is a clinical study titled "Longitudinal Endpoint Assessment of Disease Burden in HD". LEAD-HD is intended to collect and analyze self-reported health information from individuals with Huntington Disease (HD) or prodromal HD participating in a 24-month longitudinal natural history study using remote technologies.

What is the current status of trial NCT06475898?

This trial is currently recruiting. The enrollment target is 600 participants. The study started on 2024-06-25. Estimated completion is 2026-12.

What conditions does trial NCT06475898 study?

This clinical trial studies the following conditions: Huntington Disease.

Who is sponsoring clinical trial NCT06475898?

This trial is sponsored by Huntington Study Group, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06475898 being conducted?

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

Similar trials for Huntington Disease

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 NCT06475898's enrollment target sits among peer trials

600 8th of 35 higher than 27 of 35 other Huntington Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Huntington Disease 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

  • NCT00004317 · 600 participants · Phase 4

    Pyrimethamine, Sulfadiazine, and Leucovorin in Treating Patients With Congenital Toxoplasmosis

  • NCT00209235 · 600 participants · NA

    Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral Assessments

  • NCT01473784 · 600 participants · NA

    Transoral Robotic Surgery in Treating Patients With Benign or Malignant Tumors of the Head and Neck

  • NCT01866371 · 600 participants

    High Resolution Retinal Imaging

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 NCT06475898, the US trial registry maintained by the National Library of Medicine. NCT06475898 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.