Overview

Lidocaine Spray vs Viscous Lidocaine Solution Plus Lidocaine Spray in Patients Undergoing Non-Sedated EGD

Status:
Enrolling by invitation
Trial end date:
2024-10-30
Target enrollment:
0
Participant gender:
All
Summary
This study aimed to compare the efficacy of lidocaine spray (S) alone versus lidocaine spray combined with lidocaine viscous solution (S+V) in facilitating pharyngeal observation during Non-sedating upper gastrointestinal endoscopy (UGE).
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sawanpracharak hospital
Treatments:
Lidocaine
Criteria
Inclusion Criteria:

- Patients scheduled for upper gastrointestinal endoscopy:

- Patients who are robust, without chronic illnesses, or with controlled chronic
conditions that do not adversely affect the function of any organ (American Society of
Anesthesiologists (ASA) physical status classification I-II).

Exclusion Criteria:

- Has a history of receiving painkillers or sleeping pills within 24 hours before the
endoscopy.

- Has a history of post-endoscopy nausea and vomiting.

- Patients who have undergone upper gastrointestinal endoscopy previously.

- Has chronic conditions such as epilepsy, vertigo, or mental health disorders.

- Has a history of allergy to anesthesia used in the study.

- Pregnant or currently breastfeeding.

- Refuses to participate in the study.