- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06841146
Prediction of Adhesion by Sliding Sign (Prediction)
February 19, 2025 updated by: Alev Esercan, Sanliurfa Education and Research Hospital
Prediction of Adhesion by Sliding Sign in Three or Above Cesarean Section
Sliding sign will be checked by ultrasonography by transabdominal and transvaginal route before operation of patients that had cesarean section three or more.
During cesarean section adhesions will be evaluated and noted.
The correlation and predictive values of adhesion and sliding sign will be defined in our study.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Three or more cesarean section patients will be included in our study.
In addition, inflammatory markers in complete blood count as neutrophil, lymphocyte, neutrophil/ lymphocyte ratio, pan immune inflammation value (PIV) will be recorded.
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: alev esercan, assoc.prof.
- Phone Number: 905052634609
- Email: alevesercan@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- all three and above number of cesarean section patients
Exclusion Criteria: placenta adhesion spectrum
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: patients that had cesarean section
patients had ultrasonograpy done before cesarean section and sliding sign will be defined,and at cesarean section adhesions will be defined.
|
cesarean section
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
predictive value of sliding sign for adhesions intraabdominally
Time Frame: before cesarean section
|
sensivitivity and specivitivity of sliding sign
|
before cesarean section
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
February 19, 2025
Primary Completion (Estimated)
March 1, 2025
Study Completion (Estimated)
March 31, 2025
Study Registration Dates
First Submitted
December 27, 2024
First Submitted That Met QC Criteria
February 19, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 19, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ŞEAH/CS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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