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NCT05667324 · ClinicalTrials.gov registry record · Phase 4

Septorhinoplasty Post-operative Pain Control With SPG Nerve Block

A Phase 4 study of Deviated Nasal Septum, sponsored by University of Florida.

Completed
Registry status
Phase 4
Development phase
50
Enrollment target
1
Study location

NCT05667324: Completed Phase 4 study of Deviated Nasal Septum, sponsored by University of Florida.

NCT05667324 is a Phase 4 study of Deviated Nasal Septum that has completed, run by University of Florida. The registered enrollment target is 50 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05667324, a Phase 4 study of Deviated Nasal Septum, has completed, sponsored by University of Florida.

COMPLETED
Registry status
Phase 4
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

Maxillary nerve blocks have been shown to significantly reduce post-operative pain and analgesic intake during the 24-hour period following sinus surgery. This randomized, double-blinded, placebo-controlled study will investigate blocks of the pterygopalatine fossa using a suprazygomatic approach during septorhinoplasty surgery. It is the investigator's hypothesis that this technique will result in decreased post-operative pain and opioid use, and the morbidity associated with it.

Primary Outcome

To assess if bilateral sphenopalatine nerve blocks can decrease post operative pain scores on a scale from 0-10, with a 0 meaning no pain and 10 meaning extreme pain. Pain scores were assessed on post operative days 1, 3 and 5.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Dexamethasone
  • DRUG Ropivacaine

Study Locations (1)

Florida

  • UF Health of University of Florida - Gainesville

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2023-04-12
Est. Completion 2025-02-28
Phase Phase 4
University of Florida

1,106 total trials

What the finished NCT05667324 record still lists

NCT05667324 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).

The record links to 1 condition, with Deviated Nasal Septum appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT05667324 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT05667324 about?

NCT05667324 is a clinical study titled "Septorhinoplasty Post-operative Pain Control With SPG Nerve Block". Maxillary nerve blocks have been shown to significantly reduce post-operative pain and analgesic intake during the 24-hour period following sinus surgery. This randomized, double-blinded, placebo-controlled study will investigate blocks of the pterygopalatine fossa using a suprazygomatic approach du...

What is the current status of trial NCT05667324?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2023-04-12. Estimated completion is 2025-02-28.

What conditions does trial NCT05667324 study?

This clinical trial studies the following conditions: Deviated Nasal Septum.

What interventions are being tested in trial NCT05667324?

The interventions under investigation include: Placebo (DRUG), Dexamethasone (DRUG), Ropivacaine (DRUG).

Who is sponsoring clinical trial NCT05667324?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05667324 being conducted?

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

Similar trials for Deviated Nasal Septum

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 NCT05667324's enrollment target sits among peer trials

50 1255th of 2000 higher than 679 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

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Source: ClinicalTrials.gov NCT05667324, the US trial registry maintained by the National Library of Medicine. NCT05667324 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.