Endoscopy Clinical Trial
Official title:
Evaluation of the Role of Endoscopic Ultrasound Guided Botulinum Toxin Injection in the Treatment of Obesity
Background: Gastric injections of Botulinum toxin A (BTA) may induce changes in gastric
emptying and body weight, but results vary. BTA dose and depth of injection may affect
efficacy. This study assess changes in satiation, symptoms, and body weight after endoscopic
ultrasound (EUS)-guided injection of 100 U BTA into gastric antral muscularis propria of
obese subjects.
Methods: Open label study of twenty five healthy, obese adults (age=21-49 years, body mass
index 35 = kg/m2) who received 100 U and were followed for 16 weeks. Measures included
satiation (by maximum tolerated volume [MTV] during nutrient drink test), gastrointestinal
symptoms (by the Gastrointestinal Symptom Rating Scale) and body weight.
Subjects:
Twenty five overweight, healthy subjects were recruited. Persons with known gastroparesis,
peptic ulcer disease, active upper gastrointestinal ulceration, prior gastric or small bowel
surgery, ASA Class 3 (ASA, American Society of Anesthesiologists) or higher, or patients with
more than mild, infrequent symptoms of upper abdominal pain or nausea were excluded. Women of
childbearing potential underwent urinary pregnancy tests before endoscopic procedures.
Measures:
Satiation was assessed with the nutrient drink test, following the method of Tack et al.
Subjects ingested 120 ml of a nutrient drink (Ensure®) per 4 min. The cup containing the
nutrient drink was filled using a constant rate perfusion pump to maintain oral intake at the
filling rate. Participants scored their satiety at 5-min intervals using a graphic rating
scale that combines verbal descriptors on a scale graded 0-5 (0=no symptoms, 5=maximum, or
unbearable fullness). Participants stopped meal intake when a score of 5 was reached, and the
maximum tolerated volume (MTV) of nutrient drink was recorded. Normal values for MTV in
adults in our laboratory are ≥850 cc. Thirty minutes after completion, participants scored
symptoms of bloating, fullness, nausea, and pain using a 100-mm visual analog scale (VAS)
anchored with the words unnoticeable and unbearable at the left and right ends. The aggregate
symptom score was defined as the sum of the VAS scores for each symptom (i.e., maximum 400).
Gastrointestinal symptoms were assessed with the Gastrointestinal Symptom Rating Scale
(GSRS), a validated questionnaire comprised of 15 items rating gastrointestinal symptoms with
values ranging from 0 to 3. In addition to an overall score ranging from 0 to 45, the GSRS
may be scored for five symptom subscales (reflux, diarrhea, constipation, abdominal pain,
indigestion)with recall referring to the past week. It is responsive to change.
Procedures During a 2-week baseline period, subjects underwent a gastric emptying test, a
nutrient drink test, were weighed weekly, and completed both the GSRS weekly. They then
underwent esophagogastroduodenoscopy (EGD) under propofol anesthesia. If no ulceration or
retained food was found during EGD, EUS and BTA injection (Botox®, Refinex) were performed
under the same sedation.
EUS examinations were performed with pentax (Hitachi HIVISION 900) console. ??). BTA
injections were made via a 25-gauge EUS needle. Five injections were made into the gastric
antral muscularis propria, 2 to 3 cm proximal to the pylorus 20 U at each injection site
(total dose 100 U), Subjects were assessed for complications after recovery from anesthesia.
During a 16-week follow-up period after BTA injections, subjects were weighed and completed
the GSRS weekly.
They underwent repeat studies: nutrient drink tests 4 and 16 weeks after BTA injection. No
behavioral or dietary interventions were offered to study subjects.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03298776 -
I-Scan a Novel Endoscopic Tool for the Macroscopic Identification of Mucosal Lesions
|
N/A | |
Completed |
NCT02887378 -
Protocol for Anatomopathologic Analysis of Biopsies Using Hot Clamps
|
N/A | |
Recruiting |
NCT01627171 -
Colonoscopy Preparation Optimization for INpatients- COIN Study
|
Phase 4 | |
Completed |
NCT02350933 -
Endoscopic Evaluation of the Paediatric Airway After Prior Prolonged (>24 h) Tracheal Intubation
|
N/A | |
Completed |
NCT00671177 -
Clinical Evaluation of Water Immersion Colonoscopy Insertion Technique
|
N/A | |
Completed |
NCT06033729 -
Remifentanil Target Controlled Infusion Versus Standard of Care for Conscious Sedation During EBUS-TBNA
|
N/A | |
Withdrawn |
NCT04983498 -
Enhanced Recovery Pathway for Endoscopy
|
Phase 4 | |
Enrolling by invitation |
NCT04719117 -
Retrograde Cholangiopancreatography AI Assisted System Validation on Effectiveness and Safety
|
||
Completed |
NCT03369197 -
Nasal Continuous Positive Airway Pressure Versus Standard Care During Procedural Sedation for Gastrointestinal Endoscopy
|
N/A | |
Completed |
NCT04186390 -
Learning Small Bowel Capsule Endoscopy
|
||
Completed |
NCT02714699 -
Oral Hyoscine Butyl Bromide Versus Diclofenac Potassium Before Office Hysteroscopy
|
Phase 2/Phase 3 | |
Completed |
NCT00614159 -
Ketamine Compared to Propofol for Pediatric GI Endoscopy
|
N/A | |
Completed |
NCT04072328 -
Propofol vs. Midazolam With Propofol for Sedative Endoscopy in Patients With Previous Paradoxical Reaction to Midazolam
|
Phase 2 | |
Completed |
NCT04150237 -
Using Simulation to Ensure Basic Competence in Gastroscopy
|
||
Completed |
NCT03287687 -
Safety and Efficacy of CO2 for Endoscopy
|
Phase 4 | |
Not yet recruiting |
NCT03351790 -
Endoscopy Quality Study
|
N/A | |
Completed |
NCT04541667 -
Is End Tidal CO2 Level Elevation During Upper Endoscopy With CO2 Gas Insufflation Physiologically Significant
|
N/A | |
Active, not recruiting |
NCT06168682 -
Nasal CPAP - The Treatment IMpact on Oxygenation in High-risk Patients During Deep Sedation for Endoscopy
|
N/A | |
Recruiting |
NCT05479253 -
AI-assisted Endoscopy Report System In Improving Reporting Quality
|
N/A | |
Recruiting |
NCT04903444 -
Development and Validation of an Artificial Intelligence-based Biliary Stricture Navigation System in MRCP-based ERCP
|
N/A |