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NCT05184192 · ClinicalTrials.gov registry record · Phase 2

Efficacy of Gabapentin for Post-Covid-19 Olfactory Dysfunction

A Phase 2 study, sponsored by Washington University School of Medicine.

Completed
Registry status
Phase 2
Development phase
68
Enrollment target

NCT05184192: Completed Phase 2 study, sponsored by Washington University School of Medicine.

NCT05184192 is a Phase 2 study that has completed, run by Washington University School of Medicine. The registered enrollment target is 68 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (49% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05184192, a Phase 2 study, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
Phase 2
Development phase
68 participants
Enrollment target

Study Summary

This study will investigate the efficacy of oral gabapentin in olfactory improvement following Covid-19- associated olfactory dysfunction. This is a randomized, double-blinded, placebo-controlled trial.

Primary Outcome

The primary outcome measure was the treatment response rate following the 8-week FD phase as determined by the CGI-I. The CGI-I is a modified 7-point Likert scale of -perceived change. Response options include: (1) much better, (2) somewhat better, (3) slightly better), (4) neither better nor worse, (5) slightly worse, (6) somewhat worse, (7) much worse. The response rate was defined as the number of participants self-reporting at least "slightly better" divided by the number of participants in

Interventions

  • DRUG Placebo
  • DRUG Gabapentin gelatin capsules 300mg

Trial Details

FieldValue
Enrollment Target 68 participants
Start Date 2022-01-10
Est. Completion 2023-08-29
Phase Phase 2

What the finished NCT05184192 record still lists

NCT05184192 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (49% lower).

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

NCT05184192 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05184192 about?

NCT05184192 is a clinical study titled "Efficacy of Gabapentin for Post-Covid-19 Olfactory Dysfunction". This study will investigate the efficacy of oral gabapentin in olfactory improvement following Covid-19- associated olfactory dysfunction. This is a randomized, double-blinded, placebo-controlled trial.

What is the current status of trial NCT05184192?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 68 participants. The study started on 2022-01-10. Estimated completion is 2023-08-29.

What interventions are being tested in trial NCT05184192?

The interventions under investigation include: Placebo (DRUG), Gabapentin gelatin capsules 300mg (DRUG).

Who is sponsoring clinical trial NCT05184192?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05184192's enrollment target sits among peer trials

68 967th of 2000 higher than 1,027 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT05184192, the US trial registry maintained by the National Library of Medicine. NCT05184192 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.