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NCT02998151 · ClinicalTrials.gov registry record · Early Phase 1

Neurophysiological and Acute Pharmacological Studies in FXS Patients

A Early Phase 1 study of Fragile X Syndrome, sponsored by Children's Hospital Medical Center, Cincinnati.

Completed
Registry status
Early Phase 1
Development phase
29
Enrollment target
1
Study location

NCT02998151 is a Early Phase 1 study of Fragile X Syndrome that has completed, run by Children's Hospital Medical Center, Cincinnati. The registered enrollment target is 29 participants, below the 100-participant average among 16 other Fragile X Syndrome trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02998151, a Early Phase 1 study of Fragile X Syndrome, has completed, sponsored by Children's Hospital Medical Center, Cincinnati.

COMPLETED
Registry status
Early Phase 1
Development phase
29 participants
Enrollment target
1
Study location

Study Summary

The aim of this study is to utilize neurophysiologic assessments, behavioral measures and clinical measures to assess how much deficits associated with Fragile X Syndrome from pre-dose to post-dose using pharmacology.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Acamprosate
  • DRUG Minocycline
  • DRUG Lovastatin
  • DRUG Baclofen

Study Locations (1)

Ohio

  • Cincinnati Children's Hospital Medical Center - Cincinnati

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2016-01
Est. Completion 2020-11
Phase Early Phase 1

What the Registry Record Tells You About NCT02998151

The ClinicalTrials.gov registry entry for NCT02998151 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 29 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 100-participant average among 16 other Fragile X Syndrome trials with a reported enrollment target (71% lower). The listed sponsor is Children's Hospital Medical Center, Cincinnati, which has 571 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Fragile X Syndrome appearing as the primary indexed condition, and to 5 interventions - of which Placebo is the first listed.

NCT02998151 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT02998151 about?

NCT02998151 is a clinical study titled "Neurophysiological and Acute Pharmacological Studies in FXS Patients". The aim of this study is to utilize neurophysiologic assessments, behavioral measures and clinical measures to assess how much deficits associated with Fragile X Syndrome from pre-dose to post-dose using pharmacology.

What is the current status of trial NCT02998151?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 29 participants. The study started on 2016-01. Estimated completion is 2020-11.

What conditions does trial NCT02998151 study?

This clinical trial studies the following conditions: Fragile X Syndrome.

What interventions are being tested in trial NCT02998151?

The interventions under investigation include: Placebo (DRUG), Acamprosate (DRUG), Minocycline (DRUG), Lovastatin (DRUG), Baclofen (DRUG).

Who is sponsoring clinical trial NCT02998151?

This trial is sponsored by Children's Hospital Medical Center, Cincinnati, which has 571 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02998151 being conducted?

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

Similar trials for Fragile X Syndrome

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

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