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NCT05556889

Safety and Analgesic Efficacy of a Modified Auriculotemporal Nerve Block

Recruiting now NA Last updated 31 May 2024
What this trial tests

NA trial testing a modified auriculotemporal nerve blockade in Safety and Efficacy in 252 participants. Currently enrolling.

Timeline
1 January 2022
Primary endpoint
30 December 2024
30 December 2024

Quick facts

Lead sponsorTongji Hospital
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment252
Start date1 January 2022
Primary completion30 December 2024
Estimated completion30 December 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Tongji Hospital

Who can join

Adults 18 to 65, any sex, with Safety and Efficacy or Scalp Nerve Block. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

1. Efficacy of a modified auriculotemporal nerve blockade for patients undergoing supratentorial craniotomy 2. Safety of a modified auriculotemporal nerve blockade for patients undergoing supratentorial craniotomy

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Safety and Efficacy

Currently open trials in the same condition.

Other Tongji Hospital 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/NCT05556889.

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