The Treatment Outcomes of Cesarean Scar Pregnancy
ConditionCesarean Scar Pregnancy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorWomen's Hospital School Of Medicine Zhejiang University
About this trial
A prospective randomized controlled study evaluating the impact of various treatment modalities for cesarean scar pregnancy on treatment outcomes and pregnancy outcomes
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Women over 18 years old with a history of cesarean section
Ultrasound diagnosis of cesarean scar pregnancy
No severe internal or external diseases, such as liver disease, kidney disease, cardiovascular disease, cerebrovascular disease, etc., and able to tolerate surgery
Disqualifiers
Women under the age of 18
CSP patients who have received treatment in other hospitals
Trial population
A prospective randomized controlled study evaluating the impact of various treatment modalities for cesarean scar pregnancy on treatment outcomes and pregnancy outcomes. The excisional surgeries were conducted via excision of the cesarean scar pregnancy and closure of the uterine incision through a transvaginal approach or hysteroscopy-assisted laparoscopic approach. Conservative surgeries refer to the removal of intrauterine pregnancy tissues through ultrasound-guided vacuum aspiration or hysteroscopic surgery.
Trial design
Design model
Case-control
Time perspective
Prospective
Treatments tested in this trial
different surgical treatment
Other interventionThe excisional surgeries were conducted via excision of the cesarean scar pregnancy and closure of the uterine incision through a transvaginal approach or hysteroscopy-assisted laparoscopic approach. Conservative surgeries refer to the removal of intrauterine pregnancy tissues through ultrasound-guided vacuum aspiration or hysteroscopic surgery.
Treatment groups
82 Participants
are divided into 2 treatment groupsGroup A: excisional surgery group1 intervention
Group B: conservative surgery group1 intervention
Trial outcomes
Primary outcomes
1
successful surgical treatment
successful treatment rate after surgery
Time frame
One day after surgerySecondary outcomes
1
complication
severe complication rate after surgery
Time frame
One day after surgeryOther outcomes
1
subsequent pregnancy rate
subsequent pregnancy rate after surgery
Time frame
Up to 24 months after surgery without contraception and the time since the last menstrual period is 4 weeks or more.2
CSP recurrence rate
CSP recurrence rate after surgery
Time frame
Up to 24 months after surgery without contraception3
pregnancy interval
pregnancy interval after surgery
Time frame
Up to 24 months (the time interval between the cessation of contraception after surgery and the time of last menstrual period of the subsequent pregnancy)Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov