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Prediction of Pelvic Adhesions at Repeat Cesarean Delivery

Predictive Value of Striae Gravidarum Severity and Cesarean Scar Characteristics for Pelvic Adhesions at Repeat Cesarean Delivery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02943148
Enrollment
300
Registered
2016-10-24
Start date
2016-11-30
Completion date
2018-06-30
Last updated
2020-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Decrease Maternal Morbidity

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.

Interventions

OTHERDavey score for striae gravidarum

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Rate of of abdominal adhesions in relation to striae scoring system30 min

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026