search
Back to results

The Role of TVSG and HS in Determining Endometrial Pathologies

Primary Purpose

Abnormal Uterine Bleeding

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Transvaginal ultrasound
Hysteroscopy
Sponsored by
Sisli Hamidiye Etfal Training and Research Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Abnormal Uterine Bleeding focused on measuring transvaginal ultrasonography, hysteroscopy, abnormal uterine bleeding

Eligibility Criteria

21 Years - 51 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • patients who have no history of hysteroscopy and curettage,
  • patients who have no history of ovulatory dysfunction
  • women who have active vaginal bleeding.

Exclusion Criteria:

  • presence of genital infections/PID
  • presence of pregnancy
  • presence of vaginal or cervical pathology causing vaginal bleeding
  • women who are receiving hormonal treatment (COC/HRT)
  • patients formerly diagnosed with endometrial pathology
  • patients having coagulopathy
  • women who are using intrauterine device.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Other

    Arm Label

    Transvaginal ultrasound

    Hysteroscopy

    Arm Description

    Transvaginal ultrasound was applied 216 women with abnormal uterine bleeding.The transvaginal ultrasound diagnoses were compared with the received endometrial samples.

    Hysteroscopy was also performed under general anesthesia.Hysteroscopy was performed by a single operator (NNY).The operator and two supervising endoscopists were blinded to the ultrasound results.After the hysteroscopy, endometrial sampling was also done. The diagnoses were compared with the received endometrial samples.

    Outcomes

    Primary Outcome Measures

    accuracy of diagnostic performance transvaginal ultrasonography and hysteroscopy
    The main outcome variable of the study was accuracy of diagnostic performance of transvaginal ultrasonography and hysteroscopy in premenopausal and menopausal women with abnormal uterin bleeding .

    Secondary Outcome Measures

    Full Information

    First Posted
    February 15, 2018
    Last Updated
    February 22, 2018
    Sponsor
    Sisli Hamidiye Etfal Training and Research Hospital
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT03441087
    Brief Title
    The Role of TVSG and HS in Determining Endometrial Pathologies
    Official Title
    Ultrasound and Hysteroscopy's Place on the Diagnosis of Abnormal Uterin Bleeding
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    January 1, 2011 (Actual)
    Primary Completion Date
    December 31, 2011 (Actual)
    Study Completion Date
    December 31, 2011 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Sisli Hamidiye Etfal Training and Research Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Although hysteroscopy (HS) and transvaginal ultrasonography (TVSG) are methods in the diagnosis of AUB, there is some suspicion about their efficacy. The aim of this study was to determine the efficacy and safety of HS and TVSG on diagnosing abnormal uterine bleeding(AUB) .216 women admitted to the investigators clinic (Sisli Ethal Training and Research Hospital, Obstetrics and Gynecology Department Obstetrics Service ) between 21-51 years of age. These patients were divided into two groups; menopause (71women) and pre-menopause (145 women). HS and endometrial sampling were performed both groups after TVSG.The success of these methods was assessed by kappa analysis

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Abnormal Uterine Bleeding
    Keywords
    transvaginal ultrasonography, hysteroscopy, abnormal uterine bleeding

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Non-Randomized
    Enrollment
    216 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Transvaginal ultrasound
    Arm Type
    Other
    Arm Description
    Transvaginal ultrasound was applied 216 women with abnormal uterine bleeding.The transvaginal ultrasound diagnoses were compared with the received endometrial samples.
    Arm Title
    Hysteroscopy
    Arm Type
    Other
    Arm Description
    Hysteroscopy was also performed under general anesthesia.Hysteroscopy was performed by a single operator (NNY).The operator and two supervising endoscopists were blinded to the ultrasound results.After the hysteroscopy, endometrial sampling was also done. The diagnoses were compared with the received endometrial samples.
    Intervention Type
    Device
    Intervention Name(s)
    Transvaginal ultrasound
    Intervention Type
    Device
    Intervention Name(s)
    Hysteroscopy
    Primary Outcome Measure Information:
    Title
    accuracy of diagnostic performance transvaginal ultrasonography and hysteroscopy
    Description
    The main outcome variable of the study was accuracy of diagnostic performance of transvaginal ultrasonography and hysteroscopy in premenopausal and menopausal women with abnormal uterin bleeding .
    Time Frame
    up to 12 month

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    21 Years
    Maximum Age & Unit of Time
    51 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: patients who have no history of hysteroscopy and curettage, patients who have no history of ovulatory dysfunction women who have active vaginal bleeding. Exclusion Criteria: presence of genital infections/PID presence of pregnancy presence of vaginal or cervical pathology causing vaginal bleeding women who are receiving hormonal treatment (COC/HRT) patients formerly diagnosed with endometrial pathology patients having coagulopathy women who are using intrauterine device.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nefise Nazlı YENIGUL, MD
    Organizational Affiliation
    Sisli Etfal Research and Training hospital, Obstetrics and gynecology department Istanbul, Marmara Turkey
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Learn more about this trial

    The Role of TVSG and HS in Determining Endometrial Pathologies

    We'll reach out to this number within 24 hrs