Pregnancy and Childbirth
Conditions
Interventions
control group
study group
Sponsors
suez canal university
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: age between18–45 years old; (2) being pregnant at the time of recruitment; (3) presence of a keloid scar from a previous caesarean section; ( 4) planned caesarean section for the current pregnancy. Women of all ethnicities with a keloid scar following a previous caesarean section will be eligible to participate in the study.
Exclusion criteria
Exclusion criteria: having a previous caesarean section with no keloid scar.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine efficacy of Surgical excision and subdermal injection of triamcinolone acetonide for prevention of keloid scars after caesarean section . 2- To asses side effects of the surgical excision and subdermal injection of triamcinolone acetonide at the time of caesarean section (recent scar) | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effect of surgical excision and subdermal injection of triamcinolone acetonide on symptoms of depression in women with keloid scars . 2-To investigate patients ‘satisfaction with the treatment and their perception with the changes in their keloid scar after surgical excision and subdermal injection of triamcinolone acetonide . | — |
Countries
Egypt
Contacts
Public Contactomima taha
suez canal university
Outcome results
None listed