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Oral Losartan in Prevention of Post-ERCP Paancreatitis

Evaluation of Oral Losartan in the Prevention of Post-ERCP Pancreatitis

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04049734
Enrollment
100
Registered
2019-08-08
Start date
2015-01-31
Completion date
2017-03-31
Last updated
2019-08-09

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

Conditions

Post-ERCP Acute Pancreatitis

Brief summary

Oral losartan given in the dose of 50 mg one hour before ERCP was studied in the prevention of post ERCP pancreatitis in 50 patients indicated for ERCP in comparison with another 50 patients underwent ERCP without receiving oral losartan.

Interventions

DRUGoral losatan

50 mg of oral losartan one hour before the ERCP once

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Any adult patient indicated for ERCP * Patients with obstructive jaundice. * Patients with dilated intra-hepatic or extra-hepatic bile ducts due to malignant or benign lesions.

Exclusion criteria

* Patients refusing to undergo the procedure or signing the informed consent * Patients with clinically evident acute pancreatitis before the procedure * Patients with previous endoscopic or surgical sphincterotomy * Patients with current use of losartan * Patients who are allergic or hypersensitive to losartan or hydro soluble contrast solutions * Patients receiving NSAIDS within a week prior to assessment * Patients with severe co-morbid conditions as cardiovascular disease, renal failure or decompensated liver cirrhosis.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with development of acute pancreatitis24 hoursNumber of participants with development of abdominal pain and elevated serum amylase and/or lipase

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026