ClinicalTrials.gg
Status unknownNCT05112029Updated Nov 8, 2021

Metabolic Profile and Adipokine Levels in Young Hyperandrogenemic Females

An observational study in Hyperandrogenism, Obesity and Metabolic Disease, sponsored by Medical University of Gdansk. Status unknown at 1 site in Poland. Open to female participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2021-11-08.

Sponsored by Medical University of Gdansk · Observational

The sponsor has not verified this record recently (last verified Oct 2021), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
40
Ages
18 Years to 40 Years
Sex
Female
01

Study summary

Assessement of basic metabolic profile and adipokine levels in young hyperandrogenemic females.

02

Conditions studied

  • Hyperandrogenism
  • Obesity
  • Metabolic Disease
  • Metabolic Syndrome
03

In context

Hyperandrogenism

81 studies on the registry are indexed under Hyperandrogenism; 22 are open to participants now.

This study's planned enrollment of 40 is below the median of 135 across 26 observational studies indexed under Hyperandrogenism.

Browse Hyperandrogenism studies →

Lead sponsor

Medical University of Gdansk is the lead sponsor of 133 studies on the registry; 46 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Hyperandrogenemic females admitted for additional assessment due to medical reasons.

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

  • hyperandrogenemia
  • to participate
  • female sex
  • age 18-40 years old

Exclusion criteria

Exclusion Criteria:

  • male sex
  • no consent given
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. Basic metabolic profile.

    Serum lipids, uric acid, fasting glucose and insulin.

    Time frame: Day of blood testing - no further assessment planned (observational study).

  2. Adipokines.

    Time frame: Day of blood testing - no further assessment planned (observational study).

07

Study locations

1 of 1 sites recruiting
  • Department of Endocrinology and Internal Medicine, Medical University of Gdansk
    Gdańsk, Poland
    Recruiting
    • Agata Berlińska, MD · Contact
    • Renata Świątkowska-Stodulska, MD PhD · Principal investigator
    • Agata Berlińska, MD · Principal investigator
    • Dominika Okroj, MD · Sub investigator
    • Katarzyna Blatch, MD · Sub investigator
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Sep 2021 (actual). Primary completion is estimated for Jun 2022, 9 months after the start.

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

Registered
Oct 14, 2021
First posted
Nov 8, 2021
StartActual
Sep 22, 2021
Primary completionEst.
Jun 2022
CompletionEst.
Jun 2022
Last update
Nov 8, 2021
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 Nov 8, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05112029
Responsible party
Sponsor
First posted
Nov 8, 2021
Start date
Sep 22, 2021
Primary completion
Jun 2022 (estimated)
Completion
Jun 2022 (estimated)
Last update
Nov 8, 2021

Study contacts

Agata Berlińska, MD
Contact
agata.berlinska@gumed.edu.pl
+48 58 584 48 05
Dominika Okroj, MD
Contact
dominika.okroj@gumed.edu.pl
+48 58 584 48 05
Renata Świątkowska-Stodulska, MD PhD
study director · Medical University of Gdansk
Agata Berlińska, MD
principal investigator · Medical University of Gdansk

Oversight

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

Not currently enrolling

This study is status unknown, as verified in Oct 2021. You cannot join it, but the record below documents what was studied.

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Discussion

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