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Non Alcoholic Fatty Liver DiseaseNCT07768956

Effects of Turkish Coffee and Green Tea in Fatty Liver Disease

A study testing green tea, Turkish Coffee and mediterranean diet in people with Non Alcoholic Fatty Liver Disease, run by Okan University at 1 site in Turkey (Türkiye).

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

Non-alcoholic fatty liver disease (NAFLD) is a common liver condition associated with metabolic disorders and lifestyle factors. This study aims to evaluate the effects of Turkish coffee and green tea consumption in addition to a Mediterranean diet intervention on liver fat content, biochemical parameters, and… Read more about this study

Who is it for?
Ages 19 to 65 years
Conditions the study is for
Non Alcoholic Fatty Liver Disease
What is being tested?
green tea, Turkish Coffee and mediterranean diet
Could I receive a placebo?
No, everyone receives an active treatment
How many people
47 participants
Where
1 siteTurkey (Türkiye)
Study dates
25 Sep 2024to 15 Aug 2025
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 19 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Participants aged 19-65 years with a diagnosis of non-alcoholic fatty liver disease (NAFLD).
  • Not using medications for diabetes, dyslipidemia, or rheumatoid arthritis.
  • Not using dietary supplements.
  • No dietary program followed within the previous month.
  • No severe psychiatric disorders.
  • Willingness to participate in the study and provide informed consent.

Who cannot join

  • Presence of diabetes, dyslipidemia, or rheumatoid arthritis.
  • Alcohol consumption.
  • Positive hepatitis B surface antigen (HBsAg), hepatitis C positivity, autoimmune hepatitis, liver cirrhosis, toxic hepatitis, or alanine aminotransferase (ALT) levels ≥10 times the upper limit of normal.
  • Presence of liver malignancy or hepatic decompensation.
  • Use of systemic corticosteroids or methotrexate within the previous 6 months.
  • Pregnancy or lactation.
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  • Regular use of dietary supplements.
  • Following a dietary program within the previous month.
  • Presence of severe psychiatric disorders.
  • High daily consumption of tea and coffee.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Istanbul Dr. Lutfi Kirdar City Hospital

    Istanbul, Istanbul, 34865

Other trials in Turkey (Türkiye)

About this study

Official title: The Effects of Turkish Coffee and Green Tea Consumption on Liver Steatosis Level and Biochemical Parameters in Individuals With Non-Alcoholic Fatty Liver Disease

Non-alcoholic fatty liver disease (NAFLD) is a common liver condition associated with metabolic disorders and lifestyle factors. This study aims to evaluate the effects of Turkish coffee and green tea consumption in addition to a Mediterranean diet intervention on liver fat content, biochemical parameters, and anthropometric measurements in individuals with fatty liver disease.

Participants received a 12-week Mediterranean diet program and were assigned to groups consuming Turkish coffee, green tea, or no additional beverage intervention. Changes in liver ultrasonography findings, liver enzymes, metabolic parameters, and body measurements were evaluated before and after the intervention.

Read the detailed description

Non-alcoholic fatty liver disease (NAFLD), recently included under the broader term metabolic dysfunction-associated steatotic liver disease (MASLD), is the most common chronic liver disease worldwide and is strongly associated with obesity, insulin resistance, and metabolic abnormalities. Lifestyle modification, particularly dietary interventions, is considered the cornerstone of NAFLD management.

This randomized controlled study was designed to investigate the effects of Turkish coffee and green tea consumption combined with a Mediterranean diet intervention on liver steatosis, biochemical parameters, and anthropometric measurements in individuals diagnosed with fatty liver disease.

Participants were assigned to three groups: a Turkish coffee group, a green tea group, and a control group. All participants received a 12-week Mediterranean diet intervention. In addition to the dietary intervention, the Turkish coffee group consumed Turkish coffee twice daily, while the green tea group consumed green tea three times daily. The control group continued with the Mediterranean diet without additional beverage intervention.

Before and after the 12-week intervention, participants were evaluated for liver steatosis using ultrasonography, liver function tests (including alanine aminotransferase [ALT], aspartate aminotransferase [AST], and gamma-glutamyl transferase [GGT]), metabolic parameters, and anthropometric measurements.

The aim of this study is to determine whether Turkish coffee and green tea consumption as an adjunct to a Mediterranean diet may have beneficial effects on liver fat accumulation and metabolic health parameters in individuals with fatty liver disease.

Being tested
green tea, Turkish Coffee, mediterranean diet
Keywords
non-alcoholic fatty liver disease, Turkish coffee, green tea, diet therapy
Medical subject headings
Non-alcoholic Fatty Liver Disease

What participants receive

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

  • green teaBehavioural

    Participants consumed green tea three times daily as an adjunct to a Mediterranean diet intervention for 12 weeks.

  • Turkish CoffeeBehavioural

    Participants consumed Turkish coffee twice daily as an adjunct to a Mediterranean diet intervention for 12 weeks.

  • mediterranean dietBehavioural

    participants received a Mediterranean diet intervention without additional Turkish coffee or green tea consumption for 12 weeks.

Study groups in NCT07768956
Study groupRoleWhat they receive
Mediterranean Diet + Green TeaExperimentalParticipants received a Mediterranean diet intervention and consumed green tea three times daily as an adjunct to the diet for 12 weeks.
Receives: Behavioral: green tea; Behavioral: mediterranean diet
Mediterranean Diet + Turkish CoffeeExperimentalParticipants received a Mediterranean diet intervention and consumed Turkish coffee twice daily for 12 weeks
Receives: Behavioral: Turkish Coffee; Behavioral: mediterranean diet
Mediterranean Diet ControlActive comparatorParticipants received a Mediterranean diet intervention without additional Turkish coffee or green tea consumption for 12 weeks.
Receives: Behavioral: mediterranean diet

What is being measured

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

  1. Change in liver steatozis grade by abdominal Ultrasonography

    Liver steatosis was assessed by abdominal ultrasonography and graded as Grade 0 (no steatosis), Grade 1 (mild steatosis), Grade 2 (moderate steatosis), and Grade 3 (severe steatosis). Higher grades indicate greater severity of hepatic steatosis.

    Measured: Baseline and 12 weeks

Secondary outcomes (3)
  1. Change in Alanine Aminotransferase (ALT) Level (U/L)

    Changes in serum alanine aminotransferase (ALT) (U/L) were measured at baseline and after 12 weeks intervention to evaluate changes in liver function.

    Measured: Baseline and 12 Weeks

  2. Change in Aspartate Aminotransferase (AST) Level (U/L)

    Changes in serum aspartate aminotransferase (AST) levels (U/L) were measured at baseline and after the 12-week intervention.

    Measured: Baseline and Week 12

  3. Change in Gamma-Glutamyl Transferase (GGT) Level (U/L)

    Changes in serum gamma-glutamyl transferase (GGT) levels (U/L) were measured at baseline and after the 12-week intervention.

    Measured: Baseline and Week 12

Timeline

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

  1. First posted17 Aug 2026
  2. Study start25 Sep 2024
  3. Primary completion15 Aug 2025
  4. Study completion15 Aug 2025

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
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a 12-week, three-arm, parallel-group randomized controlled study. Participants were assigned to one of three groups: Turkish coffee group, green tea group, or control group. All participants received a Mediterranean diet intervention. In addition, the Turkish coffee group consumed Turkish coffee twice daily, and the green tea group consumed green tea three times daily. The control group received the Mediterranean diet intervention without additional beverage supplementation.
Masking
None (open label)
Enrolment
47 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07768956
Sponsor's protocol ID
OKANU-NAFLD-2026-001
Status last verified
Jul 2026
First submitted
4 Aug 2026
Last updated
17 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing green tea, Turkish Coffee and mediterranean diet in people with Non Alcoholic Fatty Liver Disease, run by Okan University at 1 site in Turkey (Türkiye).

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 6 inclusion and 10 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 17 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 Turkey (Türkiye). 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. 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?

Change in liver steatozis grade by abdominal Ultrasonography (time frame: Baseline and 12 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 17 Aug 2026.

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