Infertility Clinical Trials

Find Infertility Clinical Trials Near You

Preliminary Clinical Application Study of Saline Infusion Onohysterography in Structure of Cesarean Scar Surgery

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

This study selected patients who underwent cesarean section and were scheduled to undergo Saline Infusion Sonohysterography (SIS) for evaluating the structure of the incision. Clinical characteristics and clinical symptoms were collected. Combined with hysteroscopy, MRI, conventional ultrasound and SIS examination results, the study analyzed the detection rate of cesarean section diverticula by SIS, the changes in diverticulum size and the diagnostic efficacy of residual muscle layer thickness at the incision site. The surgical methods and clinical symptom improvement of patients with CSD after surgery were followed up for half a year to one year. The study aimed to clarify the guiding value of SIS in clinical decision-making and patient prognosis for patients, and to analyze the etiological relationship between the true incidence of CSD and clinical complications. Thus, it provided evidence-based basis for clinical events of cesarean section surgery → CSD → CSD complications → surgical treatment of CSD → patient prognosis, promoting the progress of precise diagnosis and treatment of female reproductive health.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 20
Maximum Age: 50
Healthy Volunteers: t
View:

• More than 6 months after cesarean delivery;

• Presenting with clinical symptoms-including abnormal uterine bleeding, dysmenorrhea, prolonged menstrual spotting, or secondary infertility;

• Requiring saline infusion sonohysterography (SIS) to evaluate the cesarean scar.

Locations
Other Locations
China
Tang-Du Hospital
RECRUITING
Xi'an
Contact Information
Primary
Li Zhang, MD
lilyzhang319_20@hotmail.com
86-29-84778860
Backup
Jing Ma, MM
178937707@qq.com
+86-15529398263
Time Frame
Start Date: 2023-01-01
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 300
Treatments
This group of patients received appropriate treatment based on the presence or absence of diverticul
The treatment plan was determined by the attending physician according to clinical guidelines and was strictly independent of this observational study protocol.
Sponsors
Leads: Tang-Du Hospital

This content was sourced from clinicaltrials.gov