Gastro-Intestinal Disorder Clinical Trial
Official title:
Effect of Palatable Lidocaine Gel Versus Dexmedetomidine on Gag Reflex During Propofol Based Sedation for Patients Undergoing Elective Upper Gastrointestinal Endoscopy. A Randomized Controlled Study
- The development of upper gastrointestinal endoscopy (UGIE) has greatly expanded the
diagnostic and therapeutic capabilities of gastroenterologists. The patient's tolerance
to procedure and endoscopist's satisfaction increase when sedation is used along with
topical pharyngeal anesthesia.
- Numerous agents are available for moderate sedation in endoscopy such as propofol,
midazolam, ketamine, fentanyl and dexmedetomidine, the choice of a particular sedative
agent depends on its availability, cost and experience of the endoscopist and patient
with that sedative agent. However, these i.v. anesthetics may be associated with
complications especially in elderly patients or in those with other comorbidities, as
apnea, hypoxia, hypotension, and paradoxical agitation, in which the patient becomes
agitated rather than sleepy from the sedation, leading to increased morbidity and the
duration of the patient's hospitalization.
- Local application of lidocaine to the oral cavity and the oropharynx, will attenuate or
even abolish the gag reflex increasing the patient's comfort thus decreasing the dose of
i.v. anesthetics with their potential complications.
- Up to our knowledge, there is no study done to evaluate the effect of palatable
lidocaine gel versus I .v dexmedetomidine on the incidence of gag reflex and total
propofol consumption during elective upper gastrointestinal endoscopy.
Upper gastrointestinal tract endoscopy (UGIE) is a valuable procedure that is commonly used
for the diagnosis of possible causes of upper gastrointestinal tract (GIT) symptoms such as
bleeding, pain, dysphagia, recurrent vomiting and reflux. Moreover, it is a safe and easy
procedure for taking biopsy samples for suspected esophageal, gastric and duodenal diseases,
grading and even ligating varices [1, 2].
UGIE is widely performed under propofol sedation that considered a safe sedation technique
and alleviates the sympathetic response to the procedure. However, gag reflex and retching
still exist in approximately 29% of those patients despite being under propofol sedation [3].
Any further trial of deepening sedation in order to minimize gagging may compromise
hemodynamics and cause respiratory depression. These complications add to the overall costs
as it increases morbidity and duration of patients' hospitalization. On the other hand,
continued gag reflex could affect the safety of the procedure, patient's tolerance and
endoscopist's satisfaction [4].
Dexmedetomidine, a short-acting selective α2‑agonist, has been used frequently as a
sedoanalgesic in many diagnostic and therapeutic procedures [5]. It provides unique sedative
activity not present in conventional sedatives so it is unlikely to cause restlessness or
respiratory depression was seen with Gaba aminobutyric acid (GABA) receptor agonists such as
propofol. Therefore it minimizes physical and emotional distress and enhances successful
completion of the procedure without remarkable gag reflex [6]. However, many clinicians may
have qualms regarding the safety profile of dexmedetomidine usage in such endoscopic
procedures due to its well known hemodynamic side effects (especially bradycardia and
hypotension) [7].
Topical pharyngeal anesthesia(TPA) has been used to avoid such complications resulting from
deepening sedation through increase i.v anesthetic doses of propofol or adjuvants that may be
used as dexmedetomidine. TPA is preferred in many centers, particularly for diagnostic
endoscopy [8, 9].
Lidocaine is widely used for TPA. The spray, gel and inhaler forms of it are commercially
available. However, application of lidocaine gel to the oral cavity and the oropharynx,
especially the base of the tongue, palate, uvula, palatopharyngeal, palatoglossal folds and
posterior pharyngeal wall will attenuate or even abolish the gag reflex while introducing the
UGIE, thus increasing the patient's comfort and tolerance to the procedure and decreasing the
dose of i.v. anesthetics with their potential complications [10, 11].
Palatable lidocaine gel is a local anesthetic that stabilizes the neuronal membrane through
hindering the ionic fluxes that initiate and transmit impulses, thereby giving a local
anesthetic action. It is a safe, well-tolerated and quite promising TPA particularly in
elderly patients and in patients with comorbidities in office-based endoscopy [12].
We hypothesize that the usage of topical palatable lidocaine gel may have an impact on
decreasing the incidence of gag reflex and total propofol consumption during upper
gastrointestinal endoscopy.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04032262 -
Parkinson's Disease and Digestive Health
|
N/A | |
Recruiting |
NCT06092866 -
Digital Versus Telephone Symptom Assessment and Triage in Primary Care
|
N/A | |
Not yet recruiting |
NCT05553717 -
Clinical Study Evaluating the Gastroprotective Effect of Carvedilol in Patients With Ischemic Heart Disease on Aspirin Therapy
|
N/A | |
Recruiting |
NCT05627882 -
Evaluation of the Impact of a Forward Viewing Scope at Time of ERCP
|
||
Recruiting |
NCT05159921 -
Can the SurgInfoBot Improve the Consent Process for Endoscopy? A Randomised Controlled Trial
|
N/A | |
Active, not recruiting |
NCT04182633 -
MTT for Children With ASD Who Have Gastrointestinal Disorders
|
Phase 2 | |
Enrolling by invitation |
NCT05889806 -
AUD Biomarkers Study (Proteomic and Genomic Analysis of Biospecimens)
|
||
Enrolling by invitation |
NCT05249270 -
Online Parent-Report Evaluation of the Effects of Processed Music
|
||
Completed |
NCT03675763 -
Efficacy of a Craniosacral Therapy Protocol in the Treatment of Infant Colic
|
N/A | |
Completed |
NCT05855174 -
Protein and Exercise-Induced Gastrointestinal Symptoms
|
N/A | |
Recruiting |
NCT05371067 -
Fructose Effect on Neuroinflammation and Feelings
|
N/A | |
Completed |
NCT05200325 -
Clinical Utility Evidence for TissueCypher®
|
N/A | |
Not yet recruiting |
NCT05846802 -
Gastroparesis Registry 4
|
||
Terminated |
NCT05470387 -
A Study to Evaluate LB1148 for Return of Bowel Function in Subjects Undergoing Bowel Resection
|
Phase 3 | |
Not yet recruiting |
NCT05664113 -
Feasibility, Safety, and Potential Efficacy of Fecal Microbiota Transplantation (FMT) for Gastrointestinal Dysfunction in Children Following Hematopoietic Cell Transplant (HCT).
|
Phase 1 | |
Not yet recruiting |
NCT06393881 -
A Study to Compare and Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of UI059 and UIC202201
|
Phase 1 | |
Recruiting |
NCT05874726 -
Biological Sample Repository for Gastrointestinal Disorders
|
||
Completed |
NCT06157034 -
Prokinetic Effect of Selected Nutraceuticals
|
N/A | |
Recruiting |
NCT04085211 -
Image-Enhanced Endoscopy in the Gastrointestinal Tract
|
||
Active, not recruiting |
NCT04293653 -
Protocol for Patients Above 75 Years Undergoing Emergency Laparotomy
|
N/A |