NCT06841146

Brief Summary

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 27, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

February 19, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 24, 2025

Completed
5 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2025

Completed
Last Updated

February 24, 2025

Status Verified

February 1, 2025

Enrollment Period

10 days

First QC Date

December 27, 2024

Last Update Submit

February 19, 2025

Conditions

Adhesions Abdominal

Keywords

adhesioncesarean sectionsliding sign

Outcome Measures

Primary Outcomes (1)

  • predictive value of sliding sign for adhesions intraabdominally

    sensivitivity and specivitivity of sliding sign

    before cesarean section

Study Arms (1)

patients that had cesarean section

ACTIVE COMPARATOR

patients had ultrasonograpy done before cesarean section and sliding sign will be defined,and at cesarean section adhesions will be defined.

Procedure: routine cesarean section

Interventions

routine cesarean sectionPROCEDURE

cesarean section

patients that had cesarean section

Eligibility Criteria

Age18 Years - 50 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • all three and above number of cesarean section patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Tissue Adhesions

Condition Hierarchy (Ancestors)

CicatrixFibrosisPathologic ProcessesPathological Conditions, Signs and Symptoms

Central Study Contacts

alev esercan, assoc.prof.

CONTACT

905052634609alevesercan@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Sanliurfa Education and Research Hospital

Study Record Dates

First Submitted

December 27, 2024

First Posted

February 24, 2025

Study Start

February 19, 2025

Primary Completion

March 1, 2025

Study Completion

March 31, 2025

Last Updated

February 24, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share