Clinical Study to Evaluate the Efficacy and Safety of Dapagliflozin in Patients With Refractory Cirrhotic Ascites

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorMansoura University

About this trial

The aim of this clinical trial is to evaluate the safety and efficacy of low dose dapagliflozin use along with standard care versus the standard care alone in improving the clinical outcomes of patients with cirrhotic refractory ascites. The main question it aims to answer is the difference in ascites control between the two groups at the end of treatment defined as:

Complete response: Disappearance of ascites. Partial response: Presence of ascites not requiring LVP. No response: Presence of ascites requiring LVP. Researchers will compare intervention group receiving dapagliflozin 5m once daily for 3 months along with standard care versus standard care group to evaluate the effectiveness and safety of dapagliflozin in refractory ascites patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults >18 years diagnosed with decompensated liver cirrhosis complicated with ascites grade 2.

Ascites cannot be mobilized despite adherence to low sodium diet of ≤88 mmol/day for ≥1 week and maximum diuretic treatment dose (spironolactone 400 mg/day or furosemide (160 mg/day).

Recurrence can't be prevented by medical therapy, Re-appearance of grade 2 or moderate ascites with moderate symmetrical abdominal distention, or grade 3 with massive ascites with marked abdominal distention within 4 weeks of initial mobilization.

Disqualifiers

Presenting blood pressure below 90/60 or history of hypotension requires vasopressor treatment.

History of recurrent urinary tract infections, defined by the occurrence of 2 or more acute UTIs within months or 3 within a year.

History of hypersensitivity to SGLT2 inhibitors.

History of diabetic ketoacidosis or presence of risk factors for DKA (i.e alcohol consumption, type 1 diabetes).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Dapagliflozin 5mg

    Drug

    Dapagliflozin 5m orally once daily for 3 months plus standard care (diuretics and Large volume paracentesis)

  • Standard care treatment

    Drug

    Diuretics and Large volume paracentesis as indicated

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: Dapagliflozin groupExperimental treatment 1 intervention
Group B: Standard care only groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Difference in ascites control between the two groups at the end of treatment

Complete response: Disappearance of ascites. Partial response: Presence of ascites not requiring LVP. No response: Presence of ascites requiring LVP.

Time frame
3 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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