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

NCT03822962 · ClinicalTrials.gov registry record · Early Phase 1

Pain Management Following Sinus Surgery

A Early Phase 1 study, sponsored by University of Nebraska.

Terminated
Registry status
Early Phase 1
Development phase
10
Enrollment target

NCT03822962: Clinical Trial Early Phase 1 study, sponsored by University of Nebraska.

NCT03822962 is a Early Phase 1 study that was terminated before completion, run by University of Nebraska. The registered enrollment target is 10 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03822962, a Early Phase 1 study, was terminated before completion, sponsored by University of Nebraska.

TERMINATED
Registry status
Early Phase 1
Development phase
10 participants
Enrollment target

Study Summary

This Study evaluates the effect of adding Non-steroidal anti-inflammatories (NSAIDs) to the post-operative pain management of sinus surgery patients and wether or not this addition reduces or eliminates the need for narcotic pain medications. Patients will be instructed to take an NSAID regimen after surgery and will be instructed to take narcotics only for breakthrough pain.

Primary Outcome

Patients will be given a Visual Analogue scale to help document their level of pain from Post-operative days 0, 1, 2, 3, 4 ,5 and the first post-operative visit with the surgeon. The patient will measure their pain score each time they take medication. The pain scale called the Wong-Baker FACES pain rating scale is a 0-10 pain scale. 0 = no hurt, 2 = hurts little bit, 4 = hurts little more, 6 = hurts even more, 8 = hurts whole lot, 10 = hurts worst. The numbers are added up to a sum and put int

Interventions

  • DRUG Ibuprofen 600Mg Tablet
  • OTHER Standard Regimen | Tylenol

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2020-11-07
Est. Completion 2023-05-30
Phase Early Phase 1
University of Nebraska

407 total trials

Why NCT03822962 stopped before completion

NCT03822962 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 2 interventions - of which Ibuprofen 600Mg Tablet is the first listed.

NCT03822962 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03822962 about?

NCT03822962 is a clinical study titled "Pain Management Following Sinus Surgery". This Study evaluates the effect of adding Non-steroidal anti-inflammatories (NSAIDs) to the post-operative pain management of sinus surgery patients and wether or not this addition reduces or eliminates the need for narcotic pain medications. Patients will be instructed to take an NSAID regimen aft...

What is the current status of trial NCT03822962?

This trial is currently terminated. It is a Early Phase 1 study. The enrollment target is 10 participants. The study started on 2020-11-07. Estimated completion is 2023-05-30.

What interventions are being tested in trial NCT03822962?

The interventions under investigation include: Ibuprofen 600Mg Tablet (DRUG), Standard Regimen | Tylenol (OTHER).

Who is sponsoring clinical trial NCT03822962?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03822962's enrollment target sits among peer trials

10 1628th of 2000 higher than 256 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 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

  • NCT00623389 · 10 participants · NA

    Evaluation of an Advanced Lower Extremity Neuroprostheses

  • NCT01241864 · 10 participants · Phase 2

    Islet Transplantation in Type 1 Diabetic Kidney Allograft

  • NCT01293214 · 10 participants · NA

    Vascularized Composite Allotransplantation for Multiple Extremity Amputations

  • NCT01474148 · 10 participants · NA

    A Neuroprosthesis for Seated Posture and Balance

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 NCT03822962, the US trial registry maintained by the National Library of Medicine. NCT03822962 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.