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Prediction of Pelvic Adhesions at Repeat Cesarean Delivery

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ClinicalTrials.gov Identifier: NCT02943148
Recruitment Status : Recruiting
First Posted : October 24, 2016
Last Update Posted : July 3, 2018
Sponsor:
Information provided by (Responsible Party):
Ahmed Mohamed Abbas, Assiut University

Brief Summary:
Several methods have been used to predict adhesions after abdominal operations. High-resolution ultrasonography, magnetic resonance imaging and scar healing properties were the methods that were evaluated in the English literature for this study. Estimating the likelihood of adhesions and related complications after prior surgery and assessing the severity of adhesion formation after surgery is not easy. Anticipating adhesions is very important to preventing complications by ensuring that the necessary preoperative preparations are in place and/or that appropriate cases are referred to a tertiary center.

Condition or disease Intervention/treatment
Decrease Maternal Morbidity Other: Davey score for striae gravidarum

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Study Type : Observational
Estimated Enrollment : 300 participants
Observational Model: Other
Time Perspective: Cross-Sectional
Official Title: Predictive Value of Striae Gravidarum Severity and Cesarean Scar Characteristics for Pelvic Adhesions at Repeat Cesarean Delivery
Study Start Date : October 2016
Estimated Primary Completion Date : September 2018
Estimated Study Completion Date : October 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Adhesions




Primary Outcome Measures :
  1. Rate of of abdominal adhesions in relation to striae scoring system [ Time Frame: 30 min ]


Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
All Women who will be admitted to our Labor Ward for emergency or elective cesarean section will be invited to participate.
Criteria

Inclusion Criteria:

  1. Women with at least previous one cesarean
  2. Full term (37- 41 weeks)
  3. Women accepted to participate in the study

Exclusion Criteria:

  1. History of pelvic inflammatory disease
  2. History of endometriosis
  3. Previous pelvic surgery other than cesarean
  4. History of wound site infections
  5. History of long corticosteroid use
  6. Women with midline incisions
  7. Women with placenta accreta
  8. Women refuse to participate in the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02943148


Locations
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Egypt
Ahmed Abbas Recruiting
Assiut, Cairo, Egypt, 002
Contact: ahmed abbas       bmr90@hotmail.com   
Sponsors and Collaborators
Assiut University

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Responsible Party: Ahmed Mohamed Abbas, Dr, Assiut University
ClinicalTrials.gov Identifier: NCT02943148     History of Changes
Other Study ID Numbers: PACS
First Posted: October 24, 2016    Key Record Dates
Last Update Posted: July 3, 2018
Last Verified: June 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes