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NCT02702024 Clinical Trial

The Effectiveness of Double Incision Technique in Uterus Preserving Surgery for Placenta Percreta

Placenta Percreta Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02702024
Other study ID # DIforPP
Secondary ID
Status Completed
Phase N/A
First received February 26, 2016
Last updated March 2, 2016
Start date January 2014

Study information
Verified date March 2016
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority Turkish: Ministry of Health
Study type Interventional

Clinical Trial Summary

Placenta percreta is a life-threatening condition that patients are under risk of massive bleeding. It readily necessitates very complicated surgery even leads to mortality. Cesarean hysterectomy is the procedure that is acknowledged worldwide, however, recent studies discussing conservative treatment with segmental resections were published. Fetal extraction and segmental resection could be performed from same (single uterine incision) or two different (double uterine incision) incisions. In this study, the investigators aimed to evaluate the effectiveness and the results of double uterine incision.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date January 2016
Accepts healthy volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Intraoperatively and pathologically confirmed diagnosis of placenta percreta

Exclusion Criteria:

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Procedure:
• Double uterine incision technique in uterus preserving surgery for placenta percreta

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary The success of segmental resection (Uterus preserving surgery) No need for hysterectomy due to massive hemorrhage or any other reason in postoperative one month Postoperative one month
See also
  Status Clinical Trial Phase
Completed NCT06267599 - Bladder Suture in Uterus-Sparing Surgery and Hysterectomy for Placenta Percreta
Recruiting NCT03638024 - Cell-free Fetal DNA Concentration in Cases of Abnormal Placental Invasion .
Active, not recruiting NCT02784886 - Cell-free Fetal DNA Circulating in the Maternal Plasma as a Marker for Morbidly Adherent Placenta N/A
Completed NCT04213755 - ROTEM in Patients With Placenta Previa
Completed NCT02728232 - Internal Iliac Artery Ligation and Abnormally Invasive Placenta N/A