CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 69 enrolled
Drug / intervention
Acetaminophen and codeine and caffeine +2 moredrug
Likely dose
Acetaminophen and codeine and caffeine 1000mgfrom 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.

Search/NCT04202406
NCT04202406N/ACompleted

Effect of Preoperative Acetaminophen-Codeine-Caffeine Combination on Inferior Alveolar Nerve Block Success in Patients With Symptomatic Irreversible Pulpitis: Randomized Double-blind Controlled Trial

Cairo University·interventional·Posted Dec 17, 2019·Updated Jul 21, 2021

In Brief

A clinical study evaluating Acetaminophen and codeine and caffeine, Acetaminophen, and 1 other intervention for Symptomatic Irreversible Pulpitis. Completed, enrolled 69 participants across 1 site.

Detailed Summary

The aim of the study is to evaluate the effect of preoperative administration of acetaminophen- codeine -caffeine combination on the success of the inferior alveolar nerve block versus bacetaminophen alone or placebo in patients with symptomatic irreversible pulpitis.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesEgypt
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedDec 17, 2019
Enrollment StartJan 9, 2021
Primary CompletionMay 10, 2021
Study CompletionJul 11, 2021
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 6.5 years ago

Interventions

Acetaminophen and codeine and caffeinedrug

The patient will receive pretreatment oral single dose of Combination of 1000mg acetaminophen- 16mg codeine- 60mg caffeine 1 hour before treatment.

Acetaminophendrug

The patient will receive pretreatment oral single dose of 1000mg acetaminophen alone 1 hour before treatment.

Placebodrug

The patient will receive placebo (starch) 1hour before treatment.