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Conservative Surgery for Placenta Accreta

Primary Purpose

Placenta Accreta

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
conservative surgery for uterus in placenta accreta
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Placenta Accreta

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Any age.
  • Any parity.
  • Previous one or more cesarean delivery.
  • Placenta previa accreta diagnosis confirmed by gray scale & color flow Doppler ultrasound in 3rd trimester. All participants had undergone abdominal ultrasound showing placenta previa anterior completely covering the internal os, with criteria suggestive of invasion by U/S

Exclusion Criteria:

  • women with medical disorder
  • women with bleeding tendency

Sites / Locations

  • Ain SHams Maternity Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Any age and parity with placenta accreta spectrum

Arm Description

After removal of the placenta, grasping the cervix from the both lips and one from each side of the cervical canal at the level of the internal os, each uterine angle and grasped the remaining lower uterine segment and Nelaton catheter was inserted inside the cervical canal to avoid closing the cervix with sutures of the uterine incision.Closing the uterine incision;taking suture at the lateral angle of the cervix and suturing it to the lower edge of the uterine angle, then another continuous suture was attached to the upper edge of the uterine incision angle[outside in-in out then out in-in out] and the same technique was repeated on the other side (cervico-isthmic sutures). controlling bleeding from the inner surface of the remaining lower uterine segment was done by 2-3 interrupted sutures between the lower uterine segment and the anterior cervical lip. closing of the uterine incision in continuous non-locking manner

Outcomes

Primary Outcome Measures

incidence rate of conserving woman's uterus
success rate of conservative surgery for placenta accreta

Secondary Outcome Measures

number of units of packed red blood cells , Fresh Frozen Plasma transfused ,postoperative haemoglobin
to assess blood loss
incidence rate of cesarean hysterectomy needed
failure of conservation , increase in blood loss
incidence of puerperal sepsis
temperature chart every 6 hours in 1st 48 hours postpartum then follow up visits 2 weeks and 6 weeks postpartum

Full Information

First Posted
July 6, 2021
Last Updated
July 27, 2021
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT04981483
Brief Title
Conservative Surgery for Placenta Accreta
Official Title
Conservative Stepwise Surgical Approach for Management of Placenta Previa Accreta: a Prospective Case Series Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
April 15, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
A stepwise surgical approach for conservative management of placenta previa accreta.
Detailed Description
a stepwise surgical approach for conservative management of placenta previa accreta to preserve women's uterus and to evaluate the efficacy and safety of this approach in controlling postpartum hemorrhage including intrapartum hemorrhage associated with conservative management.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Placenta Accreta

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Any age and parity with placenta accreta spectrum
Arm Type
Experimental
Arm Description
After removal of the placenta, grasping the cervix from the both lips and one from each side of the cervical canal at the level of the internal os, each uterine angle and grasped the remaining lower uterine segment and Nelaton catheter was inserted inside the cervical canal to avoid closing the cervix with sutures of the uterine incision.Closing the uterine incision;taking suture at the lateral angle of the cervix and suturing it to the lower edge of the uterine angle, then another continuous suture was attached to the upper edge of the uterine incision angle[outside in-in out then out in-in out] and the same technique was repeated on the other side (cervico-isthmic sutures). controlling bleeding from the inner surface of the remaining lower uterine segment was done by 2-3 interrupted sutures between the lower uterine segment and the anterior cervical lip. closing of the uterine incision in continuous non-locking manner
Intervention Type
Procedure
Intervention Name(s)
conservative surgery for uterus in placenta accreta
Intervention Description
After removal of the placenta, grasping the cervix from the both lips and one from each side of the cervical canal at the level of the internal os, each uterine angle and grasped the remaining lower uterine segment and Nelaton catheter was inserted inside the cervical canal to avoid closing the cervix with sutures of the uterine incision.Closing the uterine incision;taking suture at the lateral angle of the cervix and suturing it to the lower edge of the uterine angle, then another continuous suture was attached to the upper edge of the uterine incision angle[outside in-in out then out in-in out] and the same technique was repeated on the other side (cervico-isthmic sutures). controlling bleeding from the inner surface of the remaining lower uterine segment was done by 2-3 interrupted sutures between the lower uterine segment and the anterior cervical lip. closing of the uterine incision in continuous non-locking manner
Primary Outcome Measure Information:
Title
incidence rate of conserving woman's uterus
Description
success rate of conservative surgery for placenta accreta
Time Frame
intraoperative
Secondary Outcome Measure Information:
Title
number of units of packed red blood cells , Fresh Frozen Plasma transfused ,postoperative haemoglobin
Description
to assess blood loss
Time Frame
till 48 hours postpartum
Title
incidence rate of cesarean hysterectomy needed
Description
failure of conservation , increase in blood loss
Time Frame
intraoperative and 48 hours postpartum
Title
incidence of puerperal sepsis
Description
temperature chart every 6 hours in 1st 48 hours postpartum then follow up visits 2 weeks and 6 weeks postpartum
Time Frame
till 6 weeks postpartum

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Any age. Any parity. Previous one or more cesarean delivery. Placenta previa accreta diagnosis confirmed by gray scale & color flow Doppler ultrasound in 3rd trimester. All participants had undergone abdominal ultrasound showing placenta previa anterior completely covering the internal os, with criteria suggestive of invasion by U/S Exclusion Criteria: women with medical disorder women with bleeding tendency
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
mahmoud ghaleb, lecturer
Organizational Affiliation
ainshams university faculty of medicine
Official's Role
Study Director
Facility Information:
Facility Name
Ain SHams Maternity Hospital
City
Cairo
State/Province
Abbaseya
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No

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Conservative Surgery for Placenta Accreta

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