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Clinical Trials in Brazil / NCT07699809
Recruiting Not applicable

Administration of a 'Thirst Relieve Kit' Versus Placebo in Patients After Hospital-based Bowel Preparation for Colonoscopy and Assessment of Thirst Intensity

NCT07699809 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2025-12-08
Last updated
2026-07-13

Condition(s) studied

ThirstBowel Preparation for ColonoscopyColonoscopy

Investigational drug(s) / intervention(s)

lemon popsicleWater blister pack

lemon popsicle: The intervention group receives a "Thirst relife kit A" consisting of an encouraging message and a 60g lemon-flavored popsicle from the Jundiá® brand (Ingredients: water, sugar, glucose syrup, concentrated lemon juice, citric acid, thickeners, artificial flavoring).

Water blister pack: The control group receives a "Thirst Relife Kit B" consisting of the same encouraging message, a cotton ball, and a 10 ml blister pack of distilled water.

Study summary

The goal of this study is to evaluate whether a "thirst kit" (lemon popsicle) is effective in reducing thirst intensity in patients undergoing hospital bowel preparation for colonoscopy. The study also aims to assess the impact of the thirst kit on associated symptoms and patient satisfaction. The main questions it aims to answer are:

* Does the thirst kit reduce the intensity of thirst after bowel preparation for colonoscopy?
* Does the thirst kit reduce symptoms such as dry mouth and dry throat?
* How satisfied are patients when using the thirst kit compared to a placebo?

Researchers will compare the thirst kit to a placebo to determine its effectiveness in managing thirst during the pre-colonoscopy period.

Participants will:

* Be randomly assigned to receive either the thirst kit (lemon popsicle) or a placebo
* Use the assigned intervention during the hospital preparation period for colonoscopy
* Rate thirst intensity, associated symptoms, and satisfaction using numerical scales

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * both sexes * aged 18 years or older, with clear awareness and good cooperation * who underwent colonoscopy with hospital bowel preparation Exclusion Criteria: * any risk of oral fluid aspiration * swallowing disorders * post-operative advanced head and neck surgeries * advanced head and neck neoplasia, active oral diseases (oral mucosal lesions, stomatitis, among others) * history of gastric surgeries (gastrectomized, upper gastrointestinal tract surgeries for obesity) * use of GLP-1 analog medications and derivatives in the last 10 days according to hospital protocol (e.g., semaglutide, liraglutide, dulaglutide, tirzepatide...) * history of dementia.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hospital Sírio Libanês São Paulo São Paulo Recruiting

More Hospital Sirio-Libanes trials in Brazil

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07699809 on ClinicalTrials.gov ↗ ← All trials in Brazil