Copeptin and Thirst: Possible Predictive Markers of Effectiveness of Bariatric Surgery?
Launched by IRCCS AZIENDA OSPEDALIERO-UNIVERSITARIA DI BOLOGNA · Jan 28, 2025
Trial Information
Current as of August 21, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring how certain markers in the body, specifically copeptin and thirst levels, might help predict how effective bariatric surgery will be for people struggling with obesity. Bariatric surgery is a procedure that helps patients lose weight, and understanding these markers could improve the overall success rates of the surgery.
To be eligible for the study, participants should be between 18 and 65 years old and have a body mass index (BMI) of 40 or higher, or a BMI of 35 or higher if they have related health issues. The trial is currently looking for volunteers, and those who join will be asked to provide their consent and follow specific health guidelines throughout the process. It's important to note that individuals with certain medical conditions, like serious mental health issues or those using specific medications, may not be able to participate. If you're interested, this study could offer valuable insights into how to better treat obesity and support patients undergoing bariatric surgery.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • BMI ≥ 40 in the absence of comorbidities; BMI ≥ 35 associated with at least one comorbidity
- • Age ≥ 18 and less than or equal to 65 years
- • Written informed consent obtained
- Exclusion Criteria:
- Contraindications to bariatric surgery:
- • severe psychiatric illness in the decompensation phase;
- • drug or alcohol abuse;
- • patient unwilling to follow periodic checkups and a dietary regimen pregnancy or lactation.
- Factors that could alter ADH/copeptin:
- • Obesity induced by other endocrinopathies or medications;
- • Diabetes mellitus of any type;
- • Malignant neoplasms or ongoing acute disease;
- • Organ failure or chronic CNS and kidney disease;
- • Hydro-electrolyte alterations;
- • use of drugs that interfere with pituitary-adrenal axis, diuretics, anti-psychotics and psychopharmacological therapies, GLP1 receptor agonists, estro-progestin therapy.
About Irccs Azienda Ospedaliero Universitaria Di Bologna
IRCCS Azienda Ospedaliero-Universitaria di Bologna is a prestigious research and healthcare institution in Italy, renowned for its commitment to advancing medical science and patient care through innovative clinical research. As an IRCCS (Istituto di Ricovero e Cura a Carattere Scientifico), it integrates clinical practice with scientific research, facilitating the translation of laboratory findings into effective treatment strategies. The institution fosters a multidisciplinary approach, collaborating with various experts to conduct high-quality clinical trials aimed at improving health outcomes across a wide range of medical fields. With a strong emphasis on ethical standards and patient welfare, IRCCS Azienda Ospedaliero-Universitaria di Bologna plays a vital role in shaping the future of medicine through rigorous scientific inquiry and patient-centered care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Bologna, , Italy
Patients applied
Trial Officials
Uberto Pagotto, MD
Principal Investigator
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported