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NCT04737239 · ClinicalTrials.gov registry record

Corticosteroid Injection Effectiveness in Carpel Tunnel Patients With Negative or Mild EMG Studies

A clinical trial of Carpal Tunnel Syndrome, sponsored by Henry Ford Health System.

Recruiting
Registry status
300
Enrollment target
1
Study location

NCT04737239: Recruiting study of Carpal Tunnel Syndrome, sponsored by Henry Ford Health System.

NCT04737239 is a study of Carpal Tunnel Syndrome that is actively recruiting participants, run by Henry Ford Health System. The registered enrollment target is 300 participants, above the 208-participant average among 21 other Carpal Tunnel Syndrome trials with a reported enrollment target (44% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04737239, a study of Carpal Tunnel Syndrome, is actively recruiting participants, sponsored by Henry Ford Health System.

RECRUITING
Registry status
300 participants
Enrollment target
1
Study location

Study Summary

Carpal Tunnel Syndrome (CTS) is the most common nerve entrapment syndrome worldwide. There are currently no studies examining the effectiveness of corticosteroid injections in patients with normal (negative) EMG studies. The purpose of this study is to gain a better understanding of the duration of symptom improvement post corticosteroid injection in patients with negative or mild EMG studies. The Boston Carpal Tunnel Questionnaire will be given to patients undergoing corticosteroid injections for the treatment of carpal tunnel syndrome to assess their response to the injection. Investigators will collect data retrospectively. The Boston Carpal Tunnel Questionnaire (BCTQ) is administered as per standard protocol to all patients with CTS who have a negative or mild EMG study. The BCTQ assesses the patient's self-reported symptom severity and functional status. Investigators will analyze this data with respect to demographics as well as numbness in the median n. distribution, nocturnal numbness, weakness/atrophy of the thenar musculature, Tinel's sign, Phalen's test, loss of 2-point discrimination, Quick-Dash score, and grip strength score. The primary outcome will be the Boston Carpal Tunnel Questionnaire outcome score under the different EMG conditions.The secondary outcomes will be numbness in the median n. distribution, nocturnal numbness, weakness/atrophy of the thenar musculature, Tinel's sign, Phalen's test, loss of 2-point discrimination, QuickDash score, and grip strength score. Both outcomes will be examined in patients with negative or mild EMG readings. This information will allow orthopedic physicians to gain a better understanding of the duration of symptom improvement post-corticosteroid injection, allowing them to fine tune their treatment plans for CTS patients.

Primary Outcome

Scaled 1-5, higher scores indicate worse outcomes

Conditions Studied

Interventions

  • OTHER Corticosteroid injections for CTS treatment

Study Locations (1)

Michigan

  • Henry Ford Health System - Detroit

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2020-12-23
Est. Completion 2026-12-22
Henry Ford Health System

234 total trials

What NCT04737239 shows while recruiting

NCT04737239 is an observational study that tracks outcomes without assigning an intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, above the 208-participant average among 21 other Carpal Tunnel Syndrome trials with a reported enrollment target (44% higher).

The record links to 1 condition, with Carpal Tunnel Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Corticosteroid injections for CTS treatment is the first listed.

NCT04737239 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT04737239 about?

NCT04737239 is a clinical study titled "Corticosteroid Injection Effectiveness in Carpel Tunnel Patients With Negative or Mild EMG Studies". Carpal Tunnel Syndrome (CTS) is the most common nerve entrapment syndrome worldwide. There are currently no studies examining the effectiveness of corticosteroid injections in patients with normal (negative) EMG studies. The purpose of this study is to gain a better understanding of the duration of ...

What is the current status of trial NCT04737239?

This trial is currently recruiting. The enrollment target is 300 participants. The study started on 2020-12-23. Estimated completion is 2026-12-22.

What conditions does trial NCT04737239 study?

This clinical trial studies the following conditions: Carpal Tunnel Syndrome.

What interventions are being tested in trial NCT04737239?

The interventions under investigation include: Corticosteroid injections for CTS treatment (OTHER).

Who is sponsoring clinical trial NCT04737239?

This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04737239 being conducted?

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

Similar trials for Carpal Tunnel Syndrome

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 NCT04737239's enrollment target sits among peer trials

300 4th of 21 higher than 18 of 21 other Carpal Tunnel Syndrome trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Carpal Tunnel Syndrome 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

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Source: ClinicalTrials.gov NCT04737239, the US trial registry maintained by the National Library of Medicine. NCT04737239 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.