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Preventive Therapy With Ursodiol to Reduce the Incidence of Gallstones Formation in Patients After Bariatric Surgery

Preventive Therapy With Ursodiol to Reduce the Incidence of Gallstones Formation in Patients After Bariatric Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02319629
Enrollment
266
Registered
2014-12-18
Start date
2014-12-31
Completion date
2018-12-31
Last updated
2018-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Morbid Obesity

Keywords

Morbid obesity,, Cholelithiasis, Bariatric surgery, Ursodiol

Brief summary

Risk factor of cholelithiasis is rapid weight loss after bariatric surgery and change in the gallbladder function which is secondary to surgery. Many observational studies support this fact, and a high incidence of 28% -71% after gastric bypass surgery (RYGB) was reported in them. According to another publication, the incidence of gallbladder diseases is 5-36% after jejunoileal bypass surgery and 2.8-36% after gastric bypass surgery.

Detailed description

Study format: Prospective, randomized, blinded study. 266 candidates for sleeve gastrectomy or gastric bypass surgery due to morbid obesity with BMI range of 40-50 and aged 18-65 will be studied. The patients will be randomly divided into two groups (according to the last digit of the identity card number): 1. Treatment group will receive preventive therapy with Ursodiol 600 mg per day as of day 10 after the surgery (at the first routine visit after the surgery) and for six months or until the formation of gallstones. 2. Placebo group will receive placebo as of day 10 after the surgery (at the first routine visit after the surgery) and for six months or until the formation of gallstones.

Interventions

preventive treatment with Ursolit to reduce the incidence of gallstones formation after bariatric surgery

DRUGPlacebo

Sponsors

HaEmek Medical Center, Israel
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Candidates for sleeve gastrectomy or gastric bypass surgery due to morbid obesity with BMI range of 40 to50. * Aged 18 to 65. * No presence of gallstones. * Patients who have signed the consent form.

Exclusion criteria

* Minors, * Pregnant women, * Age over 65, * Sensitive to Ursodiol, * Gallstones, * Biliary tract pathologies, * Gallbladder wall thickening, * Patients after cholecystectomy, * Patients participating in another clinical trial.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of gallstones formation after bariatric surgerysix month\- Six months after the surgery the subjects will be invited to re-evaluation of the presence of gallstones using: 1. Clinical interview: Did he experience epigastric pain? Was he hospitalized with diagnosis of biliary colic or cholecystitis? 2. US of the upper abdomen to assess the presence of gallstones, gallbladder wall thickening or other disorder. 3. Blood tests for liver functions and lipids profile

Countries

Israel

Contacts

Primary ContactNasser Sakran, MD
sakran_as@clalit.org.il+97246494491

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026