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Study on the mechanism by which ?Np63/DGCR8-dependent microRNA-mediated SREBP1 acetylation promotes pyroptosis in GDM trophoblasts

Study on the mechanism by which ?Np63/DGCR8-dependent microRNA-mediated SREBP1 acetylation promotes pyroptosis in GDM trophoblasts

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108253
Enrollment
Unknown
Registered
2025-08-27
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gestational diabetes mellitus

Interventions

Normal pregnant controls:none
gestational diabetes mellitus:none

Sponsors

The Third Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.Age and Gender: Participants must be between 18 and 45 years of age (the specific age range may be adjusted according to the needs of the study). 2.Diagnosis and Medical History: Pregnant women who have been diagnosed with gestational diabetes mellitus (GDM). No other severe complications or comorbidities, such as severe preeclampsia or diabetic ketoacidosis. 3.Informed Consent: Participants must sign an informed consent form, clearly indicating their understanding and agreement to participate in this study. 4.Baseline Data: Participants must provide detailed medical history, medication history, family history, etc. Baseline blood glucose, haemoglobin A1c, lipid levels, etc., must meet the study requirements.

Exclusion criteria

Exclusion criteria: 1.Diseases and complications: Suffering from other diseases that may affect the study results, such as autoimmune diseases, malignant tumours, etc. Severe complications during pregnancy, such as placenta praevia, placental abruption, etc. 2.Medication: Recent use of drugs that may affect blood sugar or blood lipid levels, such as glucocorticoids, lipid-lowering drugs, etc. Currently participating in other clinical trials or studies that may affect the results of this study. 3.Inability to Cooperate: Unable to undergo regular examinations or provide necessary samples as required by the study. Communication barriers or limited understanding, unable to accurately comprehend and follow study requirements. 4.Ethical and Moral Considerations: The participant or their family members believe that participating in the study may cause discomfort or harm. The participant has already been enrolled in other similar clinical studies.

Design outcomes

Primary

MeasureTime frame
SREBP1;silence infrmation regulator,sirtuin,SIRTl;nucleotide binding oligomerization domain-like receptor protein 3, NLRP3;miRNA-128-3p;nuclear factor-erythroid 2-related factor,Nr2;glucose transporters-1,GLUT-1;DiGeorge syndrome critical region 8,DGCR8;reactive oxygen species,ROS;

Countries

China

Contacts

Public ContactHan ning

The Third Affiliated Hospital of Zhengzhou University

15515609988@163.com+86 155 1560 9988

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026