ClinicalTrials.Veeva

Menu

Remifentanil in Deep vs Moderate Neuromuscular Blocks During Surgical Pleth Index-guided Anesthesia for Laparoscopic Herniorrhaphy

A

Ajou University School of Medicine

Status

Completed

Conditions

Hernia Abdominal Wall

Treatments

Drug: Moderate neuromuscular block
Drug: Deep neuromuscular block

Study type

Interventional

Funder types

Other

Identifiers

NCT04022733
AJIRB-MED-THE-19-056

Details and patient eligibility

About

The primary purpose of this study is to compare the remifentanil requirements in deep versus moderate neuromuscular blocks during the surgical pleth index -guided anesthesia in patients undergoing laparoscopic herniorrhaphy.

Enrollment

134 patients

Sex

All

Ages

19 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • laparoscopic hernia repair

Exclusion criteria

  • patients refusal, hyperbilirubinemia, chronic pain, opioid abuse, infection, and peripheral disease

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

134 participants in 2 patient groups, including a placebo group

Moderate NMB group
Placebo Comparator group
Treatment:
Drug: Moderate neuromuscular block
Deep NMB group
Experimental group
Treatment:
Drug: Deep neuromuscular block

Trial documents
2

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems