Placenta Accreta Clinical Trial
Official title:
Comparative Study Between Intraoperative Ureteric Dissection and Preoperative Ureteric Stenting in Women With Abnormally Invasive Placenta
NCT number | NCT03763916 |
Other study ID # | 44 |
Secondary ID | |
Status | Not yet recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2018 |
Est. completion date | June 2019 |
80 Egyptian pregnant female patients will be enrolled in our prospective study. All candidates will have the diagnosis of placenta percreta [confirmed by 2D and 3D ultrasound and Doppler by senior sonographer]. All candidates will be scheduled for cesarean hysterectomy; patients will be randomized into two groups, first group will include 40 patients who will undergo cesarean hysterectomy with intraoperative ureteric dissection, and the second group will include the other 40 patients who will undergo cesarean hysterectomy with preoperative ureteric stenting.
Status | Not yet recruiting |
Enrollment | 80 |
Est. completion date | June 2019 |
Est. primary completion date | May 2019 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Parity; multiparas - Advanced gestational age more than 36 weeks - Repeated cesarean sections - Placenta previa - Abnormally invasive placenta diagnosed and confirmed by senior sonographer Exclusion Criteria: - Morbidly obese patient [BMI over 35] Severly anaemic; patients[ Hb less than 8gmLdl] Elderly females [age over 40] - Inability to insert ureteric stent |
Country | Name | City | State |
---|---|---|---|
Egypt | Kasr Alainy medical school | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | ureteric injuryoccurance of any type of ureteric injuries including partial , complete transection or inclusion in a ligature | during the operation |
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