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RecruitingNCT07833007Updated Sep 22, 2026

Metabolic Syndrome Resposne to Dietary Limitations in Familial Mediterranean Fever in Adolescents

An interventional study of low calorie diet in Familial Mediterranean Fever (FMF ) and Metabolic Syndrome, sponsored by Cairo University. Recruiting at 1 site in Egypt. Open to participants aged 13 Years to 17 Years. Per ClinicalTrials.gov, last updated 2026-09-22.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
13 Years to 17 Years
Sex
All
01

Study summary

metabolic syndrome may be prevalent in familial Mediterrean fever. Dietary limitations are main treatment in metabilc syndrome

Read the detailed description

forty metabolic syndrome participants (adolescents) with familial Mediterrean fever divided equally in to study group received low calorie diet for 3 months and control group who will no change their dietary habits

02

Conditions studied

  • Familial Mediterranean Fever (FMF )
  • Metabolic Syndrome
03

In context

Familial Mediterranean Fever

61 studies on the registry are indexed under Familial Mediterranean Fever; 27 are open to participants now.

This study's planned enrollment of 40 is close to the median of 40 across 27 interventional studies indexed under Familial Mediterranean Fever.

Browse Familial Mediterranean Fever studies →

Lead sponsor

Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.

Of its 37 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

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

04

Who can participate

Ages eligible
13 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • metabolic syndrome
  • familial mediterreanean fever

Exclusion criteria

Exclusion Criteria:

  • cardiac diseases
  • repsiratory diseases
  • tumors
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    group I

    twenty metabolic syndrome participants (adolescents) with familial Mediterrean fever will received low calorie diet for 3 months

    Behavioral: low calorie diet

  • No intervention
    group II

    Twenty metabolic syndrome participants (adolescents) with familial Mediterrean fever will no change their dietary habits for 12 weeks

Interventions

  • Behaviorallow calorie diet

    metabolic syndrome participants (adolescents) with familial Mediterrean fever will received low calorie diet for 3 months

06

What researchers measure

Primary outcomes

  1. fasting blood glcuose

    it will be assessed in plasma

    Time frame: it will be assessed after 12 weeks

Secondary outcomes

  1. body mass index

    it will be assessed while patients were on empty stomach and bladder

    Time frame: it will be assessed after 12 weeks

  2. waist circumference

    it will be assessed via tape measurement

    Time frame: it will be assessed after 12 weeks

  3. high density lipoprotein

    it will be assessed in plasma

    Time frame: it will be assessed after 12 weeks

  4. triglycerides

    it will be assessed in plasma

    Time frame: it will be assessed after 12 weeks

  5. systolic blood pressure

    it will be assessed from brachial artery

    Time frame: it will be assessed after 12 weeks

  6. diastolic blood pressure

    it will be assessed from brachial artery

    Time frame: it will be assessed after 12 weeks

  7. C reactive protein

    it will be assessed in plasma

    Time frame: it will be assessed after 12 weeks

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Aug 2026 (actual). Primary completion is estimated for Dec 2026, 4 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 16, 2026
First posted
Sep 22, 2026
StartActual
Aug 10, 2026
Primary completionEst.
Dec 15, 2026
CompletionEst.
Dec 15, 2026
Last update
Sep 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07833007
Lead sponsor
Cairo University
Responsible party
Ali Mohamed Ali ismail (lecturer of department of physical therapy for cardiovascular respiratory disorder and geriatrics, Cairo University) — Principal investigator
First posted
Sep 22, 2026
Start date
Aug 10, 2026
Primary completion
Dec 15, 2026 (estimated)
Completion
Dec 15, 2026 (estimated)
Last update
Sep 22, 2026

Study contacts

Ali Ismail, PhD
Contact
ali.mohamed@pt.cu.edu.eg
+201005154209
Ali mohamed, PhD
Contact
ali.mohamed@pt.cu.edu.eg
+201033321109
Ali MA Ismail, PHD
principal investigator · Cairo University

Oversight

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

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