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NCT02865746

Periapical Injection of Betamethasone to Control Postoperative Pain in Emergency Endodontic Care - A Randomized Double Blind Clinical Trial

Completed NA Last updated 11 August 2016
What this trial tests

NA trial testing Bethametasone in Pain in 120 participants. Completed in 1 December 2005.

Timeline
1 July 2004
Primary endpoint
1 May 2005
1 December 2005

Quick facts

Lead sponsorFederal University of the Valleys of Jequitinhonha and Mucuri
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposetreatment
Enrollment120
Start date1 July 2004
Primary completion1 May 2005
Estimated completion1 December 2005
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Federal University of the Valleys of Jequitinhonha and Mucuri

Who can join

Adults 10 to 72, any sex, with Pain. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The objective of this randomized double-blind study was to evaluate the effect of betamethasone in the control of postoperative pain in patients undergoing endodontic treatment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Pain

Currently open trials in the same condition.

Other Federal University of the Valleys of Jequitinhonha and Mucuri 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/NCT02865746.

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