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AzTrials

Polycystic Ovary SyndromeNCT07591246

Efficay of Physical Activity Program in PCOS Females With Fatty Pancrease and Thyroid Hypofunction

A study testing physical exercise program in people with Polycystic Ovary Syndrome and Non-Alcoholic Fatty Pancreatic Disease, run by Cairo University at 1 site in Egypt.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

females of polycystic ovary syndromes may complain fatty pancreaetic disorder and thyroid hypofunctions (subclinical hypothyroidism) Read more about this study

Who is it for?
Ages 20 to 40 years, women only
What is being tested?
physical exercise program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteEgypt
Study dates
7 Mar 2026to 30 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 20 to 40 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • PCOS
  • fattty pancrease (non-alcoholic)
  • subclinical hypothyroid (signifcant with thyroid stimauted horomone more than 10 mIU/L) and normal non-disordered free thyroxine horomones

Who cannot join

  • cardiac disesase
  • renal diseases
  • respiratory disease

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Ali MA Ismail, lecturer contact

01005154209

ali.mohamed@pt.cu.edu.eg

Egypt1 site, 1 recruiting
  • Cairo Unoversity

    Giza

    Ali Ismail, lecturer, 01005154209, allooka2012@gmail.com

    Recruiting

Other trials in Egypt

About this study

females of polycystic ovary syndromes may complain fatty pancreaetic disorder and thyroid hypofunctions (subclinical hypothyroidism)

Read the detailed description

females of polycystic ovary syndromes may complain fatty pancreaetic disorder and thyroid hypofunctions (subclinical hypothyroidism) will be divided to groups (twenty female for the group). groups will be treated with levothyroxine and metformin, but one of these groups will perform aerobic treadmill walking.

Being tested
physical exercise program, usual care
Medical subject headings
Polycystic Ovary Syndrome

What participants receive

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

  • physical exercise programBehavioural

    twenty females of polycystic ovary syndromes may complain fatty pancreaetic disorder and thyroid hypofunctions (subclinical hypothyroidism)will be treated with daily dose of levothyroxine in addition to daily twotimes of 500-mg metformin, and these females will perform 50 minutes of aerobic treadmill walking hrice weekly for six month.

  • usual careOther

    twenty females of polycystic ovary syndromes may complain fatty pancreaetic disorder and thyroid hypofunctions (subclinical hypothyroidism)will be treated with daily dose of levothyroxine in addition to daily two times of 500-mg metformin for six month.

Study groups in NCT07591246
Study groupRoleWhat they receive
group number 1Experimentaltwenty females of polycystic ovary syndromes may complain fatty pancreaetic disorder and thyroid hypofunctions (subclinical hypothyroidism)will be treated with daily dose of levothyroxine in addition to daily twotimes of 500-mg metformin, and these females will perform 50 minutes of aerobic treadmill walking hrice weekly for six month.
Receives: Behavioral: physical exercise program
group number 2Active comparatortwenty females of polycystic ovary syndromes may complain fatty pancreaetic disorder and thyroid hypofunctions (subclinical hypothyroidism)will be treated with daily dose of levothyroxine in addition to daily twotimes of 500-mg metformin for six month
Receives: Other: usual care

What is being measured

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

  1. Dehydroepiandrosterone

    it is a hormone involved in synthesis of sex hormones

    Measured: it will be measured after 6 months

Secondary outcomes (14)
  1. ratio of leutinzing hromone to hormone of follicels stimulatting hormones

    this ration express level of sex hormone

    Measured: it will be measured after 6 months

  2. testesterone

    it is a sex horomone

    Measured: it will be measured after 6 months

  3. body mass index

    it will be assessed on empty stomach and bladder

    Measured: it will be measured after 6 months

  4. waist circumference

    it will be assessed on umblical levels

    Measured: it will be measured after 6 months

  5. blood gluocose

    it will be assessed in fasting status

    Measured: it will be measured after 6 months

  6. glycated hemoglubin

    it is an indiactor for longterm satus of blood gloucose

    Measured: it will be measured after 6 months

  7. insulin

    it will be assessed in plasma

    Measured: it will be measured after 6 months

  8. thyroid stimualtined horomone

    it will be assessed in plasma

    Measured: it will be measured after 6 months

  9. triglyceridess

    it will be assessed in plasma

    Measured: it will be measured after 6 months

  10. low densitiy liopporotein

    it will be assessed in plasma

    Measured: it will be measured after 6 months

  11. cholesteroll

    it will be assessed in plasma

    Measured: it will be measured after 6 months

  12. high densitiy lipoporteins

    it will be assessed in plasma

    Measured: it will be measured after 6 months

  13. alanine transaminase

    it will be assessed in plasma

    Measured: it will be measured after 6 months

  14. aspartatte transaminase

    it will be assessed in plasma

    Measured: it will be measured after 6 months

Timeline

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

  1. First posted15 May 2026
  2. Study start7 Mar 2026
  3. Primary completion30 Dec 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

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
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07591246
Sponsor's protocol ID
IRB000-14233-74
Status last verified
May 2026
First submitted
9 May 2026
Last updated
15 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing physical exercise program in people with Polycystic Ovary Syndrome and Non-Alcoholic Fatty Pancreatic Disease, run by Cairo University at 1 site in Egypt.

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 3 inclusion and 3 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: looking for participants now, as of the sponsor's last update on 15 May 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 Egypt. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Ali MA Ismail, lecturer (01005154209, ali.mohamed@pt.cu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Dehydroepiandrosterone (time frame: it will be measured after 6 months). 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 15 May 2026.

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