At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 30 enrolled
Drug / intervention
Mulungu +1 moredrug
Likely dose
Mulungu 500 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Anxiety Control by Using Erythrina Mulungu in Mandibular Third Molars Extraction
In Brief
A Phase 2 clinical trial evaluating Mulungu and Placebo for Dental Anxiety and Impacted Third Molar Tooth. Completed, enrolled 30 participants across 1 site.
Detailed Summary
This study evaluated the effectiveness of the Erythrina mulungu in controlling anxiety in patients undergoing bilateral extraction of asymptomatic, impacted mandibular third molars.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDental Anxiety, Impacted Third Molar Tooth
CountriesBrazil
CollaboratorsUniversity of Campinas, Brazil
Timeline
Phase 2CompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2012
Primary CompletionJun 2012
Study CompletionNov 2012
First PostedSep 2013
TodayJul 2026
First PostedSep 23, 2013
Enrollment StartJan 1, 2012
Primary CompletionJun 1, 2012
Study CompletionNov 1, 2012
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 12.8 years ago
Interventions
Mulungudrug
500 mg/single dose/1 hour before dental surgery
Placebodrug
500 mg/single dose/1 hour before dental surgery