Intravenous Infusion of Lidocaine in Gastroscopy

  • STATUS
    Recruiting
  • participants needed
    130
  • sponsor
    Shandong University
Updated on 16 February 2024
lidocaine
gastroscopy

Summary

Intravenous infusion of lidocaine significantly reduces incidence of bucking when perfomed gastroscopy.

Description

This study divide patients into two groups, the patients in lidocaine group will be given lidocaine; the control group will be given placebo .the primary endopiont was to investigate whether intravenous lidocaine can reduce incidence of bucking and movement in sedation of gastroscopy.

Details
Condition Sedation
Age 18years - 80years
Treatment Placebo, Lidocaine
Clinical Study IdentifierNCT04439773
SponsorShandong University
Last Modified on16 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

patients aged >18 years who were scheduled for ERCP at Qilu hospital

Exclusion Criteria

patients with ASA (American Society of Anesthesiologists) Class 4 or 5, pre-
existing hypoxemia (SpO2 <90%), hypotension (systolic blood pressure <90 mm
Hg), bradycardia (HR<50 beats/min), uncontrolled hypertension (SBP >170 mm Hg
diastolic blood pressure>100 mm Hg), severe renal or liver failure, pregnancy
or lactation, allergy to lidocaine, atrioventricular block, epilepsy, and
inability to give informed consen
Clear my responses

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.