Placenta Accreta&Its Complications in Placenta Previa Cases

Placenta Accreta in Placenta Previa Anterior Clinical Trial

Official title:

Incidence of Placenta Accreta & it's Complications in Cases of Previous Cesarean With Placenta Previa Anterior

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT02606474
• Other study ID #: Obgyn. . .
• Status: Not yet recruiting
• Phase: N/A
• First received: November 7, 2015
• Last updated: November 13, 2015
• Start date: November 2015
• Est. completion date: March 2016

Study information

• Verified date: November 2015
• Source: Kasr El Aini Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Egypt: Ministry of Higher Education
• Study type: Observational

Clinical Trial Summary

Cases of previous cesarean with placenta previa anterior underwent cesarean section. Placenta accreta is diagnosed during cesarean section &confirmed by pathology. All complications are monitored in cases with placenta accreta and without.

Description:

100 cases of gestational age 30 weeks or more with placenta previa anterior with previous one or more cesarean section will be enrolled. History,examination &routine investigations will be taken. Colour doppler will be done to diagnose cases with suspected placenta accreta. Pre & postoperative Hb concentration will be taken. Cases with nonseparation of the placenta will be diagnosed as accreta & confirmed by pathology. Operative time & complications like bladder or intestinal injury will be noted. All data will be analyzed.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: March 2016
• Est. primary completion date: March 2016
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• all pregnant women more than 30 weeks with previous one or more cesarean section with placenta previa anterior

Exclusion Criteria:

• pregnant with unscarred uterus

• scars other than cesarean section

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

• Placenta Accreta
• Placenta Accreta in Placenta Previa Anterior
• Placenta Previa

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Kasr El Aini Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of patients with placenta accreta.		3 months	No
Primary	Number of patients with bladder injury.		3 months	No
Primary	Number of patients with intestinal injury.		3 months	No
Primary	Number of patients with cesarean hysterectomy.		3 months	No
Primary	Number of deaths.		3 months	No