Working... Menu
Trial record 5 of 7 for:    Recruiting, Not yet recruiting, Available Studies | Stretch marks

Prediction of Pelvic Adhesions at Repeat Cesarean Delivery

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT02943148
Recruitment Status : Recruiting
First Posted : October 24, 2016
Last Update Posted : July 3, 2018
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

Layout table for study information
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

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
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.

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 identifier (NCT number): NCT02943148

Layout table for location information
Ahmed Abbas Recruiting
Assiut, Cairo, Egypt, 002
Contact: ahmed abbas   
Sponsors and Collaborators
Assiut University

Layout table for additonal information
Responsible Party: Ahmed Mohamed Abbas, Dr, Assiut University 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