Lower Uterine Segment Thickness and Term Pain,Previous Cesarean Section

Evaluation of Lower Uterine Segment Thickness in Pregnant Women Presenting With Term Pain and Previous Cesarean Section

the purpose of the researchers; The aim of this study is to evaluate the consistency of niche dimensions measured by ultrasonography with visual measurement of the surgeon during the operation of the patient when presenting with pain in her current pregnancy.

If patients who have had previous cesarean section present to the emergency department with pain or NST pain, a panic occurs immediately for operation. Purpose of researchers; The aim of this study is to investigate whether a really fine determination of the thickness of the old incision line is associated with full-thickness rupture or incomplete rupture, which appears to be an operation, and if a relationship is found, there is a limit for this thickness.

Study Overview

• Status: Completed
• Conditions: Cesarean Section Complications; Cesarean Section; Dehiscence
• Intervention / Treatment: Procedure: Measure niche thickness with ultrasound

• Study Type: Observational
• Enrollment (Actual): 100

Contacts and Locations

Study Locations

• Turkey
  • Istanbul, Turkey, 33404
    • Kanuni Sultan Suleyman Training and Research Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 45 years (Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

• Sampling Method: Non-Probability Sample

Study Population

In Pregnant Women with Term Pain and Previous Cesarean Section; Patients with visual evaluation of the lower uterine segment thickness and ultrasound

Description

Inclusion Criteria:

• Patients with a previous cesarean section
• Those in term gestational week (37-42 weeks)
• Those who apply to the emergency with pain

Exclusion Criteria:

• Birden fazla sezaryen geçirilmiş öyküsü olan hastalar
• Önceden geçirilmiş uterin cerrahisi olan hastalar
• Miad olmayan gebeler
• Plesantal yerleşim patolojısı olan gebeler

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
patients with previous cesarean section; presenting to the emergency department with pain, previous cesarean section; Patients measured niche thickness before operation	Procedure: Measure niche thickness with ultrasound; in patients with previous cesarean section who applied to the emergency department with pain and underwent surgery; Measure niche thickness before operation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Measure niche thickness with ultrasound	Ultrasonography of Lower Uterine Segment Thickness in Pregnant Women Presenting with Term Pain and Previous Cesarean Section It will be given in mm.	1 day
Measure niche thickness with visual evaluation of the surgeon	Measured Lower Uterine Segment Thickness by Visual Evaluation of Pregnant Women Presenting with Term Pain and Previous Cesarean Section no rupture have full coat rupture have incomplete rupture; will be valued as.	1 day

Collaborators and Investigators

• Sponsor: Kanuni Sultan Suleyman Training and Research Hospital

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2019
• Primary Completion (Actual): January 1, 2020
• Study Completion (Actual): January 1, 2020

Study Registration Dates

• First Submitted: August 24, 2019
• First Submitted That Met QC Criteria: August 24, 2019
• First Posted (Actual): August 28, 2019

Study Record Updates

• Last Update Posted (Actual): January 18, 2020
• Last Update Submitted That Met QC Criteria: January 14, 2020
• Last Verified: January 1, 2020

More Information

Terms related to this study

• Other Study ID Numbers: 2019.05.117

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No