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CompletedNCT07461012Updated Mar 10, 2026

Impact of Garlic on the Clinical Outcome in Chronic Hemodialysis Patients

An interventional study of Dried garlic powder (Garlic extract) - Allium sativum. in Hemodialysis, Endothelial Dysfunction and CKD, sponsored by Ain Shams University. Completed at 1 site in Egypt. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-10.

Sponsored by Ain Shams University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Oct 2025, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
58
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Chronic kidney disease (CKD) is an irreversible condition marked by reduced kidney function or structural abnormalities lasting over three months, affecting a significant portion of the global population. It leads to a cycle of complications including albuminuria, anemia, mineral bone disorders, inflammation, oxidative stress, and accumulation of uremic toxins. These factors contribute to endothelial dysfunction (ED) and elevate the risk of cardiovascular diseases (CVDs), which are the primary cause of death in end stage kidney disease (ESKD) patients, especially those undergoing hemodialysis (HD). Hemodialysis further aggravates systemic inflammation and oxidative stress, increasing levels of cytokines like IL-6, TNF-α, and CRP. Endocan, a proteoglycan secreted by endothelial cells in response to inflammation, is a promising biomarker for ED and CVD risk, with levels that correlate with CKD severity. Garlic (Allium sativum) contains bioactive compounds with proven anti-inflammatory, antioxidant, and endothelial protective effects. This trial was suggested based on a study that has reported that giving 400 mg of garlic extract twice a day for 8 weeks in peritoneal dialysis patients resulted in significant reduction in IL-6, CRP and ESR. This study aims to investigate the effect of Garlic on Endothelial dysfunction and inflammation in chronic hemodialysis patients via assessment of Endocan as an endothelial dysfunction marker and IL-6 as an inflammation marker.

02

Conditions studied

  • Hemodialysis
  • Endothelial Dysfunction
  • CKD
  • Inflammation

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03

In context

Inflammation

3,438 studies on the registry are indexed under Inflammation; 629 are open to participants now.

This study's enrollment of 58 is above the median of 50 across 2,436 interventional studies indexed under Inflammation.

Browse Inflammation studies →

Lead sponsor

Ain Shams University is the lead sponsor of 1,876 studies on the registry; 423 are open to participants now.

Of its 32 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adult patients aged above 18 years with confirmed diagnosis of CKD.
  • Patients on HD for at least 3 months before enrollment.
  • Patients not participating in other clinical trials.
  • Physically stable.

Exclusion criteria

Exclusion Criteria:

  • Patients diagnosed with digestive diseases as ileal bypass.
  • Patients with a history of hemorrhagic disorders or taking medications like warfarin.
  • Patients sensitive to garlic.
  • Patients with history of alcohol or drug abuse.
  • Patients receiving other anti-inflammatory medications (e.g. use of vitamin E at a dose higher than 60 IU per day or vitamin C higher than 500 mg per day)
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
58 participants (actual)

Study arms

  • Experimental
    Group A (Garlic Group)

    It consists of 29 patients who will receive a tablet containing 300 mg dried garlic powder three times daily for 12 weeks. (Tomex® plus, ATOS Pharma, Egypt) besides the standard treatment.

    Dietary Supplement: Dried garlic powder (Garlic extract) - Allium sativum.

  • No intervention
    Group B (control Group)

    It consists of 29 patients who will receive the standard treatment.

Interventions

  • Dietary supplementDried garlic powder (Garlic extract) - Allium sativum.

    A tablet containing 300 mg dried garlic powder

06

What researchers measure

Primary outcomes

  1. endocan

    To evaluate the impact of Garlic on endothelial dysfunction in chronic hemodialysis patients via assessment of Endocan.

    Time frame: 12 weeks

  2. interleukin-6

    To evaluate the impact of Garlic on inflammation in chronic hemodialysis patients via assessment of IL-6 marker.

    Time frame: 12 weeks

Secondary outcomes

  1. safety of garlic in CHD patients

    To evaluate the safety of Garlic in patients on HD by monitoring any adverse effects that may occur.

    Time frame: 12 weeks

  2. (KDQOL™-36) questionnaire

    To evaluate the impact of Garlic on quality of life in CHD patients

    Time frame: 12 weeks

07

Study locations

1 site
  • faculty of pharmacy Ain Shams university
    Cairo, Egypt
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07461012
Lead sponsor
Ain Shams University
Responsible party
martina ezzat (Teaching assistant at faculty of pharmacy Ain Shams university, Ain Shams University) — Principal investigator
First posted
Mar 10, 2026
Start date
Oct 1, 2025
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025
Last update
Mar 10, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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