Prevalence of Cesarean Section Niche in Women With Unexplained Abnormal Uterine Bleeding

NCT ID: NCT03130387

Last Updated: 2017-04-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

95 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-01-01

Study Completion Date

2017-04-20

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Prevalence of Cesarean Section Niche in women With Unexplained Abnormal Uterine Bleeding

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Prevalence of Cesarean Section Niche as diagnosed by office hysteroscopy and transvaginal sonography in women With Unexplained Abnormal Uterine Bleeding

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cesarean Section; Dehiscence Abnormal Uterine Bleeding

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Hysteroscopic examination for patients with AUB
Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Office hysteroscopy

Examinatin with Office hysteroscope for women with abnormal uterine bleeding who had a history of previous cesarean section

Group Type OTHER

Office Hysteroscope

Intervention Type DEVICE

Diagnosis of C.S niche in patients wit AUB by office hysteroscope

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Office Hysteroscope

Diagnosis of C.S niche in patients wit AUB by office hysteroscope

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Patients with a history of cesarean section who are complaining of abnormal uterine bleeding with the following criteria :

* Normal complete blood count apart from paramaters of anemia
* Not using drugs affecting coagulation profile
* Bleeding is not related to pregnancy
* Not using intrauterine contraceptive devices or hormonal contraceptives
* By ultrasonography : no abnormalities in the pelvis e.g benign or malignant tumors , ovarian cysts or tumors
* No evidence of cervical abnormalities as cause of bleeding with cervical examination or cervical smears

* If the patient refused the technique ( office hysteroscopy )
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ahmed Elsayed Hassan Elbohoty

Head of Early Cancer Detection Unit

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

IEldawa

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.