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Use of QRX-3 for Acute Tubular Necrosis Type of Renal Failure in Hospitalized Patients ( QRX-3 in ARF)

E

Ebima Clifford Okundaye

Status and phase

Not yet enrolling
Phase 3
Phase 2

Conditions

Acute Renal Failure (ARF)
Acute Tubular Necrosis

Treatments

Drug: QRX-3

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

Use of QRX-3 in hospitalized patients with pediatric and adult patients with acute tubular necrosis renal failure

Enrollment

500 estimated patients

Sex

All

Ages

10 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalized patients
  • presence of Acute renal failure
  • Nephrologist diagnosis of Acute tubular necrosis or fractional excretion of sodium of >2%
  • willingness to participate

Exclusion criteria

High risk of bleeding Absence of hydronephrosis or obstructive uropathy Absence of baseline dialysis use single kidney status

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

500 participants in 2 patient groups, including a placebo group

Use of QRX-3 in addition to standard therapy
Experimental group
Description:
QRX-3 drug orally as twice daily in addition to standard conventional therapy will be given to this group for 28 days
Treatment:
Drug: QRX-3
control group
Placebo Comparator group
Description:
placebo twice daily will be given to this group in addition to standard therapy
Treatment:
Drug: QRX-3

Trial contacts and locations

1

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Central trial contact

Ebima Okundaye, MD

Data sourced from clinicaltrials.gov

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