At a glance
ClinicalIndex Comparison RecordN/ACompleted· 160 enrolled
Drug / intervention
BIS monitordevice
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.
Does Bispectral Index Improve Surgical Conditions During Fast Track Gynecological Benign Laparoscopies
In Brief
A clinical study evaluating BIS monitor for Consciousness Monitors and Laparoscopy. Completed, enrolled 160 participants across 1 site.
Detailed Summary
This study investigates whether BIS monitor assisted anesthesia improves surgical space conditions during gynecological benign laparoscopic procedures. Half of participants will receive BIS monitor assisted anesthesia, while the other half will receive anesthesia without BIS monitor.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsConsciousness Monitors, Laparoscopy
CountriesDenmark
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
Enrollment StartApr 2019
First PostedApr 2019
Primary CompletionMar 2021
Study CompletionMar 2021
TodayJul 2026
First PostedApr 11, 2019
Enrollment StartApr 1, 2019
Primary CompletionMar 8, 2021
Study CompletionMar 11, 2021
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 7.2 years ago
Interventions
BIS monitordevice
Participants allocated to the intervention group will receive TIVA anesthesia adjusted by the BIS monitoring in addition to clinical signs of poor anesthesia.