Skip to content

Interrupted Versus Continuous Subcuticular Skin Suturing in Elective Cesarean Section.

Comparative Study Between Interrupted and Continuous Subcuticular Skin Suturing in Women Undergoing Elective Cesarean Section. A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03120806
Enrollment
169
Registered
2017-04-19
Start date
2017-04-16
Completion date
2017-12-20
Last updated
2021-12-23

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

Conditions

Cesarean Section Wound

Brief summary

Non-diabetic pregnant women who undergo elective CS will be randomized into two groups: group I included women who has their skin closed with subcuticular interrupted mattress suture using non-absorbable polypropylene, and group II included women who has their skin closed with subcuticular continous suture using the same suture material

Detailed description

Non-diabetic pregnant women who undergo elective CS will be randomized into two groups: group I included women who had their skin closed with subcuticular interrupted mattress suture using non-absorbable polypropylene, and group II included women who had their skin closed with subcuticular continous suture using the same suture material.

Interventions

PROCEDUREInterrupted subcuticular skin closure

skin is closed with interrupted mattress subcuticular sutures using non-absorbable polypropylene after elective cesarean section

PROCEDUREcontinuous subcuticular skin closure

skin is closed with continuous subcuticular sutures using non-absorbable polypropylene after elective cesarean section

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
19 Years to 39 Years
Healthy volunteers
No

Inclusion criteria

* 18 years or older * Overall good health * Elective Cesarean section ASA class 1 or 2

Exclusion criteria

* Allergy to synthetic suture materials * Diabetes whether gestational or pregestational * use of steroid or immunosuppresive medication within last 6 month of procedure * Skin sepsis or systemic fever * BMI \> 35 * History of keloid or hypertrophic scar formation or dermatologic conditions known to impair wound healing ASA class 3 or 4

Design outcomes

Primary

MeasureTime frameDescription
wound infection10 days after surgeryoccurrence of signs of wound infection

Secondary

MeasureTime frameDescription
wound hematoma10 days after surgeryoccurrence of subcutanous hematoma
scar dehiscence10 days after surgeryoccurrence of scar dehiscence or incisional hernia
wound seroma10 days after surgeryoccurrence of seroma of wound
the need for reclosure10 days after surgeryactual gapping of wound
postoperative pain12 hours after surgerythrough visual analogue score The visual analogue scale or visual analog scale (VAS) is a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.

Countries

Egypt

Outcome results

None listed

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