Comparison of the Effect of Cyclizine Versus Metoclopramide on Gastric Residual Volume in Patient… (NCT06789614) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Comparison of the Effect of Cyclizine Versus Metoclopramide on Gastric Residual Volume in Patients Undergoing Bariatric Surgery: A Randomized Double-blinded Clinical Trial
76 participantsStarted 2025-02-18
Plain-language summary
The aim of this work is to compare the effects metoclopramide versus Cyclizine withing the context of multimodal antiemetic strategy on GRV in patients scheduled for bariatric surgery.
Who can participate
Age range18 Years – 40 Years
SexALL
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Inclusion Criteria
* â—Ź Age (18 - 40).
* Body mass index (BMI) 40 to 50 kg/m2.4
* American Society of Anaesthesiologist (ASA) - physical status III.
* Patients undergoing bariatric surgery.
* Non smokers.
Exclusion Criteria:
* â—Ź Refusal of the patient
* Deviation from fasting times
* Patients with empty stomach
* Body mass index (BMI) less than 40s kg/m2
* American Society of Anesthesiologists (ASA) physical status class IV.
* Systemic diseases may cause delayed gastric emptying (eg: myopathies and myasthenia gravis).
* Patients with gastrointestinal diseases which impact the gastric emptying such as hiatus hernia, intestinal disease and gastro-oesophageal reflux disease and patients with history of upper gastrointestinal surgeries.
* Use of other medications known to affect gastric motility or secretions (Diphenoxylate, Atropine\& Imodium) or secretions.
* Allergy to macrolide or metoclopramide. • a considerable proportion of patients with obesity have diabetes and thus, they cannot be excluded from the study. However, we would exclude patients with long standing diabetes (more than 5 years) who are likely to have delayed gastric emptying. Furthermore, this is a randomized controlled trial and the randomization usually overcomes these points and the demographic data would be displayed in the results to clarify whether there is a balance between the two groups or not.
What they're measuring
1
Estimated Gastric volume (mL)
Timeframe: 1 hour after administration of the study drugs