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Optimizing Surgical Conditions During Laparoscopic Herniotomy With Deep Neuromuscular Blockade

NCT02247466 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2019-07-02

Study results available
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Summary

The purpose of this study is to investigate surgical work space and surgical conditions in patients scheduled for laparoscopic umbilical, -linea alba and incisional herniotomy. The patients will act as their own control with evaluation of surgical work space and surgical conditions during both deep NMB and no NMB.

Conditions

  • Laparoscopic Herniotomy

Interventions

DRUG

Rocuronium and Sugammadex

Sponsors & Collaborators

  • Herlev Hospital

    lead OTHER

Principal Investigators

  • Mona Ring Gätke, MD, Ph.D. · Department of Anaesthesiology, Herlev Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2017-02-23
Completion
2017-02-23

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02247466 on ClinicalTrials.gov