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NCT03632044

Evaluation of Trigeminal Nerve Blockade

Active, enrolled Phase 4 Last updated 20 January 2026
What this trial tests

Phase 4 trial testing Ropivacaine in Mouth Abnormalities in 40 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
20 November 2018
Primary endpoint
31 May 2026
30 October 2027

Quick facts

Lead sponsorUniversity of Florida
PhasePhase 4
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment40
Start date20 November 2018
Primary completion31 May 2026
Estimated completion30 October 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Florida

Who can join

Adults 3 Months to 5, any sex, with Mouth Abnormalities or Cleft Palate. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Cleft palate repair requires high doses of opioids for pain control postop. An alternative approach is placement of nerve blocks in the pterygopalatine fossa bilaterally, blocking the maxillary nerve \& covering the entire midface. Application of bilateral suprazygomatic maxillary nerve blockade of the infraorbital nerve may provide effective analgesia for cleft lip repair, improving time to oral intake, pain control and time to hospital discharge.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Ropivacaine

Trials testing the same drug.

Other University of Florida trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03632044.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing