At a glance
ClinicalIndex Comparison RecordN/ACompleted· 105 enrolled
Drug / intervention
Remifentanildrug
Likely dose
Not stated in 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.
Comparative Study of Influence of Different Techniques of Remifentanil Titration During Functional Endoscopic Sinus Surgery Under Total Intravenous Anaesthesia (TIVA)
In Brief
A clinical study evaluating Remifentanil for Endoscopic Sinus Surgery. Completed, enrolled 105 participants across 1 site.
Detailed Summary
The aim of this randomized trial is to assess the efficacy of analgesia , compare the utility of Pupillary Dilatation Reflex (PRD), Surgical Pleth Index (SPI) for monitoring pain perception intraoperatively and their influence on intraoperative blood loss, quality of surgical field using Boezaart Bleeding Scale (BBS) in patients undergoing functional sinus surgery (FESS)
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsEndoscopic Sinus Surgery
CountriesPoland
Collaborators--
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartJun 2016
First PostedJan 2018
Primary CompletionJan 2018
TodayJul 2026
First PostedJan 4, 2018
Enrollment StartJun 1, 2016
Primary CompletionJan 15, 2018
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 8.5 years ago
Interventions
Remifentanildrug
a rate of infusion will be increased by 50% every 5 minutes