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Trial · NCT05284656

Effect of Folic Acid and/or Pentoxifylline on Patients With Chronic Kidney Disease

NCT05284656, Phase 3, Active not recruiting, Al-Azhar University; results first posted 2025-06-11

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effect of Folic Acid and/or Pentoxifylline on Patients With Chronic Kidney Disease. Trials, record NCT05284656. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05284656

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Effect of Folic Acid and/or Pentoxifylline on Patients With Chronic Kidney Disease
NCT number
NCT05284656
Status
Active not recruiting
Phases
Phase 3
Enrollment
80 participants, actual
Lead sponsor
Al-Azhar University
Conditions
Chronic Kidney Diseases
Interventions
combination of Pentoxifylline 400 MG and Folic Acid, folic acid, Pentoxifylline 400 MG
First posted
2022-03-17
Last updated
2025-06-11
Results first posted
2025-06-11

Source ClinicalTrials.gov

Registered outcomes3

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in Serum Creatinine LevelBaseline, 6 monthsChange was calculated as the value at 6 months minus the value at baseline.
SecondarySerum Ferritin in ng/ml6 monthsincrease in serum ferritin from baseline
OtherProtein/ Creatinine Ratio(P/C) (mg Protein/mg Creatinine)6 monthschange in Protein/ creatinine ratio for determination of proteinuria

Outcomes3

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Serum Creatinine LevelBaseline, 6 monthsmg/dlMEAN
SECONDARYSerum Ferritin in ng/ml6 monthsng/mlMEAN
OTHER_PRE_SPECIFIEDProtein/ Creatinine Ratio(P/C) (mg Protein/mg Creatinine)6 months

Results by group8

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Change in Serum Creatinine LevelFolic Acid Group3.118Standard Deviation 1.203mg/dl
Change in Serum Creatinine LevelPentoxifylline Group3.335Standard Deviation 1.149mg/dl
Change in Serum Creatinine LevelFolic Acid and Pentoxifylline Group3.535Standard Deviation 0.9109mg/dl
Change in Serum Creatinine LevelControl Group2.872Standard Deviation 0.8901mg/dl
Serum Ferritin in ng/mlFolic Acid Group200.6Standard Deviation 66.18ng/ml
Serum Ferritin in ng/mlPentoxifylline Group334.1Standard Deviation 230.2ng/ml
Serum Ferritin in ng/mlFolic Acid and Pentoxifylline Group245.1Standard Deviation 115.7ng/ml
Serum Ferritin in ng/mlControl Group235.3Standard Deviation 185.1ng/ml

Participant flow12

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDFolic Acid Group20
Overall StudySTARTEDPentoxifylline Group20
Overall StudySTARTEDFolic Acid and Pentoxifylline Group20
Overall StudySTARTEDControl Group20
Overall StudyCOMPLETEDFolic Acid Group20
Overall StudyCOMPLETEDPentoxifylline Group20
Overall StudyCOMPLETEDFolic Acid and Pentoxifylline Group20
Overall StudyCOMPLETEDControl Group20
Overall StudyNOT COMPLETEDFolic Acid Group0
Overall StudyNOT COMPLETEDPentoxifylline Group0

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityFolic Acid Group020
Total, all-cause mortalityPentoxifylline Group020
Total, all-cause mortalityFolic Acid and Pentoxifylline Group020
Total, all-cause mortalityControl Group020
Total, other adverse eventsFolic Acid Group020
Total, other adverse eventsPentoxifylline Group020
Total, other adverse eventsFolic Acid and Pentoxifylline Group020
Total, other adverse eventsControl Group020
Total, serious adverse eventsFolic Acid Group020
Total, serious adverse eventsPentoxifylline Group020

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
40826392DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT05284656

GET https://conductscience.org/api/trials/v1/NCT05284656/registered