Telocytes in Placental Tissues of Patients With Gestational and Pre-gestational Diabetes

Sponsor
Sohag University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05305326
Collaborator
(none)
60
1
13
4.6

Study Details

Study Description

Brief Summary

Examining the expression of telocytes in the placental tissues and umbilical cord of patients with gestational or pregestational diabetes during pregnancy compared to control.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    this is an observational study, patients with gestational or pre-gestational diabetes undergoing elective (pre-labour) Cesarean section will be asked to participate in the study. Samples of placenta and umbilical cord will be taken postpartum and will be fixed and examined using immunohistochemistry to measure abundance of telocytes in these tissues. another group of patients with non complicated pregnancies will be asked to join as a control. As the topic was never studied before, a pilot phase of 10 patients per group will be done followed by sample size collection based on SD of number of telocytes in each group. Diabetes patients will divided in 3 subgroups; Gestational diabetes and pre-gestational diabetes type 1 or 2. Each group will be further subdivided according to HBA1C level collected at the time of delivery into controlled or non controlled.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    60 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Official Title:
    Telocytes in Placental Tissues of Patients With Gestational and Pre-gestational Diabetes
    Actual Study Start Date :
    Dec 1, 2021
    Anticipated Primary Completion Date :
    Dec 31, 2022
    Anticipated Study Completion Date :
    Dec 31, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Control

    Singleton pregnancies undergoing elective pre-labour CS at gestational age (37+0 to 40+0) that are healthy

    Gestational diabetes

    Singleton pregnancies complicated with gestational diabetes undergoing pre-labour CS at gestational age (37+0 to 40+0) that are otherwise healthy

    Type 1 diabetes with pregnancy

    Singleton pregnancies complicated with Type 1 diabetes undergoing pre-labour CS at gestational age (37+0 to 40+0) that are otherwise healthy

    Type 2 diabetes with pregnancy

    Singleton pregnancies complicated with Type 2 diabetes undergoing pre-labour CS at gestational age (37+0 to 40+0) that are otherwise healthy

    Outcome Measures

    Primary Outcome Measures

    1. Telocytes [Telocytes will be assessed in placental and umbilical cord tissues fixed immediately after delivery.]

      number of telocytes per high power field detected by IHC

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • All pregnant women presented at the delivery ward in Sohag University Hospital, Sohag,
    Egypt with the following criteria:
    1. Study group: Singleton pregnancies complicated with diabetes undergoing pre-labour CS at gestational age (37+0 to 40+0). These will be divided into 3 groups according to the type of disease either Gestational diabetes (Group A), pregestational diabetes type 1 (Group B) or type 2 (Group C). 2-Control group: Singleton pregnancies undergoing elective pre-labour CS at gestational age (37+0 to 40+0) that are otherwise healthy
    Exclusion Criteria:
    • Women with history of medical co-morbidities other than diabetes are excluded from the study. This includes the following: Chronic hypertension, renal diseases, autoimmune diseases, history of organ transplantation and immunosuppressive therapy, hematological diseases, history of thrombotic events, cardiopulmonary diseases, liver diseases Acute and chronic inflammatory diseases.

    • Pregnancy induced medical disorders like: Gestational hypertension, preeclampsia, Gestational thrombocytopenia, and proteinuria.

    • Multiple pregnancies.

    • Abnormal placentation, i.e. Placenta previa and Morbidly adherent placenta.

    • Fetal anomalies.

    • vaginal deliveries and CS in labor.

    • Spontaneous delivery.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sohag Faculty of Medicine Sohag Egypt 82514

    Sponsors and Collaborators

    • Sohag University

    Investigators

    • Principal Investigator: Amr O Abdelkareem, MD, Sohag Faculty of Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Amr Othman Abdelkareem Mohammad Ahmad, Lecturer of Obstetrics and Gynecology, Sohag University
    ClinicalTrials.gov Identifier:
    NCT05305326
    Other Study ID Numbers:
    • Soh-Med-21-12-39
    First Posted:
    Mar 31, 2022
    Last Update Posted:
    Mar 31, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Amr Othman Abdelkareem Mohammad Ahmad, Lecturer of Obstetrics and Gynecology, Sohag University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 31, 2022