The Identification of Optimal Ultrasonografic Tecniques for Determining the Location , Size and the Surgical Methods of Intestinal Endometriotric Nodules

NCT04891003 | Unknown

• 1 other identifier: 2020/147
• Study Type: observational
• Target: 16
• Locations: 1 country
• Sites: 1

Brief Summary

The identification of optimal ultrasonografic tecniques for determining the location , size and the surgical methods of intestinal endometriotric nodules

Conditions

ULTRASONOGRAPHY; Endometriosis, Rectum

Keywords

Endometriosis; Diagnostic Imaging

Outcome Measures

Primary Outcomes (1)

• Endometriosis,intestinal

  Ultrrasonographic imaging of endometriosis

  4 months

Study Arms (2)

Patients Diagnosed with Endometriosis (or endometrioma alone)

Nulliparous patients who had diagnosed with endometriosis, no additional gynecological patology such as myoma uteri, polype, a history of pelvic inflammatuar disease, a history of cervical or uterine surgery, uterine anomalies

Diagnostic Test: Ultrasonography

Patients With No Gynecological Pathology

Nulliparous patients who had not diagnosed with endometriosis, no additional gynecological patology such as myoma uteri, polype, a history of pelvic inflammatuar disease, a history of cervical or uterine surgery, uterine anomalies

Diagnostic Test: Ultrasonography

Interventions

Ultrasonography DIAGNOSTIC_TEST

The identification of optimal ultrasonografic tecniques for determining the location , size and the surgical methods of intestinal endometriotric nodules.

Patients Diagnosed with Endometriosis (or endometrioma alone); Patients With No Gynecological Pathology

Eligibility Criteria

• Age: 18 Years - 45 Years
• Gender Eligibility Details: 18-45
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

Non- virgin Female Patients having only intestinal findings of deep infiltrative endometriosis aged between 18-45 years old ,

You may qualify if:

• Diagnosed with deep infiltrative endometriosis and intestinal involvement
• Treatment will be done surgically
• Patients should be nonvirgin

You may not qualify if:

• Patient has one or more extra -intestinal findings of deep infiltrative endometiosis

Sponsors & Collaborators

• Zeynep Kamil Maternity and Pediatric Research and Training Hospital: lead

Study Sites (1)

Zeynep Kamil Maternity and Childrens Training and Research Hospital

Istanbul, Uskudar, 34668, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Endometriosis

Interventions

Ultrasonography

Condition Hierarchy (Ancestors)

Genital Diseases, Female; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Genital Diseases

Intervention Hierarchy (Ancestors)

Diagnostic Imaging; Diagnostic Techniques and Procedures; Diagnosis

Central Study Contacts

Resul Karakus, MD

CONTACT

00905059164216; resul-karakus@hotmail.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Specialist

Study Record Dates

• First Submitted: May 12, 2021
• First Posted: May 18, 2021
• Study Start: February 8, 2021
• Primary Completion: March 8, 2021
• Study Completion: May 8, 2021
• Last Updated: May 18, 2021

Record last verified: 2021-05

Locations

TU (1)