- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02401841
Resolution of Neuro-muscular Block in Great Obese Patients: Neostigmine vs Sugammadex
October 19, 2015 updated by: Davide Chiumello, Policlinico Hospital
It is a observational prospective study.
The aim of this study is to compare neostigmine vs sugammadex in the resolution of neuro-muscular blockade in great obese patients.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Milan, Italy, 20122
- Recruiting
- Fondazione IRCC Ca' Granda - Ospedale Maggiore Policlinico
-
Contact:
- Davide Chiumello, MD
- Phone Number: +39 0255033237
- Email: chiumello@libero.it
-
Principal Investigator:
- Davide Chiumello, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Great obese patients undergoing videolaparoscopic surgery
Description
Inclusion Criteria:
- Great obese
- Videolaparoscopic surgery
Exclusion Criteria:
- Age under 18
- No acceptation of informed consent
- New York Heart Association > 2
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Sugammadex
Patients treated with Sugammadex
|
|
|
Neostigmine
Patients treated with Neostigmine
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Differences in neuro-muscular block resolution time between two groups
Time Frame: up to 36 months
|
up to 36 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2015
Primary Completion (Actual)
March 1, 2015
Study Registration Dates
First Submitted
March 18, 2015
First Submitted That Met QC Criteria
March 24, 2015
First Posted (Estimate)
March 30, 2015
Study Record Updates
Last Update Posted (Estimate)
October 20, 2015
Last Update Submitted That Met QC Criteria
October 19, 2015
Last Verified
October 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- Policlinico 12
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.