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Mri in Evaluation of Cesarean Section Scar Niche

A

Assiut University

Status

Unknown

Conditions

Cesarean Section; Dehiscence

Treatments

Device: MRI

Study type

Observational

Funder types

Other

Identifiers

NCT03911622
MRI in cesarean scar defects

Details and patient eligibility

About

To evaluate cesarean section scar and the lower uterine segment in non pregnant woman by MRI to :

  1. Assess the clinical symptoms like postmenstrual spotting or prolonged menstrual bleeding, dysmenorrhea, chronic pelvic pain and dyspareunia and its relation to the presence of cesarean scar defects and its characteristics .
  2. development of scoring system and correlating it with the symptoms .

Full description

With increasing cesarean section rate nowadays, the risks of cesarean scar defect (CSD) should increase. CSD is defined by ultrasound imaging as a triangular hypoechoic defect in the myometrium at the site of the previous cesarean section scar. However, patients with CSD are sometimes asymptomatic. Yet, some patients with CSD can have symptoms of abnormal uterine bleeding, pelvic pain, infertility, uterine rupture, and potential risks of adverse pregnancy outcome .There is an association between the size of a niche and postmenstrual spotting. women with a history of CS, the depth and shape of the niche were not significant factors, while a larger niche volume was described in women with postmenstrual spotting. in women with gynecological symptoms, the niches were significantly wider in women with postmenstrual spotting, dysmenorrhea or chronic pelvic pain, and the prevalence of postmenstrual spotting or prolonged menstrual bleeding was higher with a larger diameter of the niche .Magnetic resonance imaging (MRI) has recently shown a promise tool for evaluation of uterine scar thickness. As opposed to ultrasonography (USG), which is the current gold standard for this purpose, MRI reduces observer dependence and has a superior multiplanar capability.

MRI can be used for assessment of lower uterine segment. It provides accurate tissue characterization, independent of patient body mass index .

Enrollment

30 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. previous lower uterine segment cesarean section before .
  2. At least 6 months after the last cesarean section .
  3. still regularly menstruating .
  4. Absence of other gynecological disease or intrauterine lesions like endometriosis , uterine fibroid .

Exclusion criteria

  1. Post menopausal women .
  2. hysterectomy .
  3. Presence of other gynecological disease like endometriosis , uterine fibroids .
  4. any general contraindication to MRI as presence of any paramagnetic substance as pacemakers or in severely ill patients or those with claustrophobia, arrhythmic patients .
  5. intrauterine devices .
  6. bleeding tendency.

Trial contacts and locations

0

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Central trial contact

kerolos wagdy

Data sourced from clinicaltrials.gov

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