Health Condition 1: O82- Encounter for cesarean delivery without indication Health Condition 2: O82- Encounter for cesarean delivery without indication
Conditions
Interventions
Control Intervention1: POLIGLECAPRONE 25 AND
POLYAMIDE SUTURE: To compare poliglecaprone 25
monofilament suture and polyamide monofilament suture
following caesarean delivery in terms of patient sat
Sponsors
NONE
Eligibility
Inclusion criteria
Inclusion criteria: All women undergoing cesarean delivery, Previous cesarean delivery with transverse suprapubic scar, Willing to participate in the study
Exclusion criteria
Exclusion criteria: Previous cesarean delivery not using Pfannenstiel method Clinical signs of infection at the time of cesarean delivery Uncontrolled DM (HBA1C >6%) H/o keloid H/o any allergy to suture materials Any disorder requiring chronic corticosteroids/ immunosuppressants Autoimmune disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient Satisfaction of Cosmesis of Surgical Wound by using a visual analog scale before hospital discharge after surgery. 2. Scar assessment at 6 weeks of CD on the basis of Modified Hollander Cosmesis Scale. Timepoint: Patient followed 6 weeks after caesarean delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Skin closure time 2.Wound Complication Rate (Wound seroma or hematoma, wound gapping, wound infection, wound re-suturing) after CD. Timepoint: Patient followed 6 weeks after caesarean delivery | — |
Countries
India
Contacts
Public ContactPROF JAYA CHATURVEDI
AIIMS RISHIKESH
Outcome results
None listed