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NCT06316843 · ClinicalTrials.gov registry record · Phase 2

Valacyclovir Plus Celecoxib for Post-Acute Sequelae of SARS-CoV-2

A Phase 2 study of Long COVID and PASC Post Acute Sequelae of COVID 19, sponsored by Bateman Horne Center.

Completed
Registry status
Phase 2
Development phase
59
Enrollment target
1
Study location

NCT06316843 is a Phase 2 study of Long COVID and PASC Post Acute Sequelae of COVID 19 that has completed, run by Bateman Horne Center. The registered enrollment target is 59 participants, below the 2,187-participant average among 50 other Long COVID trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06316843, a Phase 2 study of Long COVID and PASC Post Acute Sequelae of COVID 19, has completed, sponsored by Bateman Horne Center.

COMPLETED
Registry status
Phase 2
Development phase
59 participants
Enrollment target
1
Study location

Study Summary

To explore the safety and efficacy of daily doses of celecoxib + valacyclovir in the treatment of patients with prolonged symptoms caused by COVID-19.

Interventions

  • DRUG Placebo
  • DRUG Valacyclovir celecoxib dose 1
  • DRUG Valacyclovir celecoxib dose 2

Study Locations (1)

Utah

  • Bateman Horne Center - Salt Lake City

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2023-10-15
Est. Completion 2024-10-31
Phase Phase 2

Sponsor

Bateman Horne Center

1 total trials

What the Registry Record Tells You About NCT06316843

The ClinicalTrials.gov registry entry for NCT06316843 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 59 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,187-participant average among 50 other Long COVID trials with a reported enrollment target (97% lower). The listed sponsor is Bateman Horne Center, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Long COVID appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT06316843 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.

Frequently Asked Questions

What is clinical trial NCT06316843 about?

NCT06316843 is a clinical study titled "Valacyclovir Plus Celecoxib for Post-Acute Sequelae of SARS-CoV-2". To explore the safety and efficacy of daily doses of celecoxib + valacyclovir in the treatment of patients with prolonged symptoms caused by COVID-19.

What is the current status of trial NCT06316843?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 59 participants. The study started on 2023-10-15. Estimated completion is 2024-10-31.

What conditions does trial NCT06316843 study?

This clinical trial studies the following conditions: Long COVID, PASC Post Acute Sequelae of COVID 19.

What interventions are being tested in trial NCT06316843?

The interventions under investigation include: Placebo (DRUG), Valacyclovir celecoxib dose 1 (DRUG), Valacyclovir celecoxib dose 2 (DRUG).

Who is sponsoring clinical trial NCT06316843?

This trial is sponsored by Bateman Horne Center, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06316843 being conducted?

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

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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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