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

NCT04256603 · ClinicalTrials.gov registry record · Phase 4

Evaluation of Initiation Time on the Efficacy of Gabapentin in Treating Neuropathic Pain in SCI

A Phase 4 study, sponsored by MetroHealth Medical Center.

Completed
Registry status
Phase 4
Development phase
27
Enrollment target

NCT04256603: Completed Phase 4 study, sponsored by MetroHealth Medical Center.

NCT04256603 is a Phase 4 study that has completed, run by MetroHealth Medical Center. The registered enrollment target is 27 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04256603, a Phase 4 study, has completed, sponsored by MetroHealth Medical Center.

COMPLETED
Registry status
Phase 4
Development phase
27 participants
Enrollment target

Study Summary

Neuropathic pain is a common complaint in those with spinal cord injury (SCI) that has a significant negative effect on quality of life. Efficacy of various treatments, however, remains controversial. There is evidence to support that gabapentin and pregabalin have some benefit in reducing neuropathic pain. Gabapentin is effective in the management of symptoms and concerns related to SCI including motor recovery, spasticity, and mood among others. This makes gabapentin an important pharmacologic intervention, which compels providers to define treatment guidelines related to its use. One aspect of which should relate to the timing of initiation of therapy. The goal of this study is to determine whether timing of initiation of treatment with gabapentin will decrease prevalence and intensity of neuropathic pain.

Primary Outcome

To determine if the time from injury influences the prevalence of neuropathic pain in acute SCI. Average of the pain during the previous 7 days on self-identified nerve or neuropathic pain levels (0-10) on 5 different measurements at the time of discharge on the Neuropathic Pain Scale. 0 being best (no pain)- 10 being worst pain. Total score range from 0 to 50.

Interventions

  • DRUG Gabapentin
  • OTHER No gabapentin

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2019-08-01
Est. Completion 2020-04-01
Phase Phase 4
MetroHealth Medical Center

76 total trials

What the finished NCT04256603 record still lists

NCT04256603 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Gabapentin is the first listed.

NCT04256603 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04256603 about?

NCT04256603 is a clinical study titled "Evaluation of Initiation Time on the Efficacy of Gabapentin in Treating Neuropathic Pain in SCI". Neuropathic pain is a common complaint in those with spinal cord injury (SCI) that has a significant negative effect on quality of life. Efficacy of various treatments, however, remains controversial. There is evidence to support that gabapentin and pregabalin have some benefit in reducing neuropath...

What is the current status of trial NCT04256603?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 27 participants. The study started on 2019-08-01. Estimated completion is 2020-04-01.

What interventions are being tested in trial NCT04256603?

The interventions under investigation include: Gabapentin (DRUG), No gabapentin (OTHER).

Who is sponsoring clinical trial NCT04256603?

This trial is sponsored by MetroHealth Medical Center, which has 76 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04256603's enrollment target sits among peer trials

27 1651st of 2000 higher than 346 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

  • NCT00912041 · 27 participants · NA

    BrainGate2: Feasibility Study of an Intracortical Neural Interface System for Persons With Tetraplegia

  • NCT02847559 · 27 participants · Phase 2

    Optune Delivered Electric Field Therapy and Bevacizumab in Treating Patients With Recurrent or Progressive Grade 2 or 3 Meningioma

  • NCT03380195 · 27 participants · NA

    Effects of Watermelon Juice on Heart Rate Recovery and Post-exercise Muscle Soreness

  • NCT03384238 · 27 participants · Phase 1

    Panitumumab-IRDye800 in Patients With Pancreatic Cancer Undergoing Surgery

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 NCT04256603, the US trial registry maintained by the National Library of Medicine. NCT04256603 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.