Cicatrix Clinical Trial
Official title:
The Efficacy of Prophylactic Use of Extract of Allium Cepae, Allantoin and Heparin in Patients With Proven Scar Development After Excision of Previous Scar
To investigate the efficacy of prophylactic use of a topical gel containing extract of allium cepae, allantoin and heparin after surgical removal of the primary cesarean scar in the second cesarean section.
120 patients who are admitted for the second cesarean delivery, not taking prophylactic
medication after the first cesarean section, whose scar development and measurements are
taken will be included in the study. First caesarean section scars will be removed
surgically for all patients. 60 out of 120 patients (treatment group) will use prophylactic
topical scar gel 2 times in a day, and remaining 60 patients (control group )won't use. The
efficacy of the drug will be evaluated by taking strict measurements of the incision and
POSAS (The Patient and Observer Scar Assessment Scale) and Vancouver Scales at 6.12 and 24
weeks.
Steps;
1. Observation of the primary cesarean scar by taking scar measurements and using
Vancouver and POSAS scales.
2. Surgical removal of the primary cesarean scar in the second cesarean section.
3. 24 weeks topical application of gel containing extract of allium cepae, allantoin and
heparin(only treatment group).
4. Observation of the skin incision at 6,12 and 24 weeks by taking scar measurements with
using Vancouver and POSAS scales.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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