CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 100 enrolled
Drug / intervention
Paracetamoldrug
Likely dose
Paracetamol 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/NCT01070732
NCT01070732Phase 4Completed

An Open-label Non-randomized Phase IV Trial of the Clinical Efficacy of Intravenously Administered 1000mg Paracetamol as Antipyretic and Analgesic Medication

University of Athens·interventional·Posted Feb 18, 2010·Updated Feb 18, 2010

In Brief

A Phase 4 clinical trial evaluating Paracetamol for Fever and Analgesia. Completed, enrolled 100 participants across 3 sites.

Detailed Summary

The present study is aiming to unravel the clinical efficacy of intravenously administered paracetamol as antipyretic and analgesic medication in various medical conditions.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsFever, Analgesia
CountriesGreece
Collaborators--

Timeline

Phase 4CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 18, 2010
Enrollment StartJan 1, 2010
Primary CompletionJan 1, 2010
TodayJul 2, 2026
Enrollment to primary: 0 daysPosted 16.4 years ago

Interventions

Paracetamoldrug

All patients will receive one single dose of 1000mg paracetamol. If considered mandatory by the attending physician, similar doses may be administered latter for a maximum period of five days. The maximum allowed daily dose is 3000mg. If the attending physician believes that after the administration of at least of three doses the desired analgesic or antipyretic effect is not achieved, he may administer any other compound in his will.