AzTrials
AzTrials

UlcerNCT07789561

Functional Food Product

A study testing pomegranate peel powder 1.5 g, pomegranate peel powder 3 g and Whole wheat muffin in people with Ulcer and Blood Tests, run by University of Lahore at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background/Objective: This study evaluated the effects of pomegranate peel powder (PPP)-enriched muffins containing 1.5 g or 2.5 g PPP on H. pylori, inflammation, oxidative stress, and gastric ulcer healing in patients with gastric ulcers. Read more about this study

Who is it for?
Ages 40 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Ulcer, Blood Tests, Liver Function Tests
What is being tested?
pomegranate peel powder 1.5 g, pomegranate peel powder 3 g and Whole wheat muffin
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
88 participants
Where
1 sitePakistan
Study dates
15 Feb 2024to 7 May 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Both male and female patients aged 40-60 years with confirmed Helicobacter pylori infection, verified through stool antigen testing along with elevated pepsinogen I and II levels, were included in the study

Who cannot join

  • pregnancy or lactation, history of gastric surgery, and current use of proton pump inhibitors. and use of medication
  • -

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Sana Noreen

    Lahore, Punjab Province, 54000

Other trials in Pakistan

About this study

Official title: Gastroprotective Effects of Pomegranate (Punica Granatum L.) Peel Powder-Enriched Functional Food in Gastric Ulcer Management

Background/Objective: This study evaluated the effects of pomegranate peel powder (PPP)-enriched muffins containing 1.5 g or 2.5 g PPP on H. pylori, inflammation, oxidative stress, and gastric ulcer healing in patients with gastric ulcers.

Conclusion: PPP-enriched muffins showed potential as a functional dietary intervention for improving antioxidant and anti-inflammatory status and supporting gastric ulcer healing.

Read the detailed description

Background/Objective: This study investigated the therapeutic potential of pomegranate peel powder (PPP), a polyphenol- and antioxidant-rich ingredient, incorporated into whole-wheat muffins at doses of 1.5 g and 2.5 g for patients with gastric ulcers. The study assessed its potential effects on H. pylori infection, gastric inflammation, oxidative stress, and mucosal healing.

Conclusion: PPP-enriched muffins were evaluated as a functional dietary intervention with potential gastroprotective, antioxidant, and anti-inflammatory properties, supporting their possible role in dietary management of gastric ulcers.

Being tested
pomegranate peel powder 1.5 g, pomegranate peel powder 3 g, Whole wheat muffin
Keywords
Punica granatum,, Gastric Ulcer, Helicobacter pylori, Functional Foods
Medical subject headings
Ulcer, Stomach Ulcer

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • pomegranate peel powder 1.5 gDietary supplement

    Whole wheat muffin enriched with pomegranate peel powder (PPP=1.5 g) + conventional Therapy

  • pomegranate peel powder 3 gDietary supplement

    Whole wheat muffin enriched with pomegranate peel powder (PPP=3g) + conventional Therapy

  • Whole wheat muffinDietary supplement

    Whole wheat muffin

Study groups in NCT07789561
Study groupRoleWhat they receive
T0: placeboPlacebo comparatorwheat muffin
Receives: Dietary Supplement: Whole wheat muffin
T1= muffin with 1.5g pppExperimentalWhole wheat muffin enriched with pomegranate peel powder (PPP=1.5g) + conventional Therapy
Receives: Dietary Supplement: pomegranate peel powder 1.5 g
T2= Muffin with 3g pppExperimentalWhole wheat muffin enriched with pomegranate peel powder (PPP=2.5g) + conventional Therapy
Receives: Dietary Supplement: pomegranate peel powder 3 g

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Liver Enzymes

    Measured: 9 weeks

Secondary outcomes (1)
  1. H.phylori

    Measured: 9 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Aug 2026
  2. Study start15 Feb 2024
  3. Primary completion5 May 2024
  4. Study completion7 May 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Participant
Enrolment
88 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07789561
Sponsor's protocol ID
REC-UOL-604/24
Status last verified
Feb 2024
First submitted
24 Aug 2026
Last updated
27 Aug 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing pomegranate peel powder 1.5 g, pomegranate peel powder 3 g and Whole wheat muffin in people with Ulcer and Blood Tests, run by University of Lahore at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Liver Enzymes (time frame: 9 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Aug 2026.

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