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The Effect of Suturing Material on Scar Healing

The Effect of Suturing Material on Scar Healing; a Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03968783
Enrollment
95
Registered
2019-05-30
Start date
2019-05-27
Completion date
2020-01-27
Last updated
2020-02-11

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

Conditions

Cesarean Section Complications, Cesarean Wound Disruption, Suture Related Complication, Wound Heal

Keywords

cesarean section, scar heal, isthmocele, suture material, saline infusion sonography

Brief summary

We want to compare the effects of 2 suture materials (monofilament and multifilament) on healing of the uterine scar after a cesarean delivery.

Detailed description

Cesarean section (CS) is the most common type of obstetric surgery. When medically justified, CS can effectively prevent maternal and perinatal mortality and morbidity however, there are many short and long-term complications of CS. One of the most common complications is the CS scar defect. CS scar defects can develop after transverse incision of the lower uterine segment, which may result in prolonged postmenstrual bleeding, spotting, pelvic pain, and infertility. Suture material is an essential part of any major surgery, serving to hold opposing tissues together and accelerate the healing process, resulting in decreased scarring of the affected areas. We sought to evaluate the effects of different synthetic absorbable suture materials on cesarean scar defect formation.

Interventions

1.0 monofilament synthetic absorbable suture for closure of the low transverse uterine incision

OTHERMultifilament suture

1.0 multifilament synthetic absorbable suture for closure of the low transverse uterine incision

Sponsors

Bezmialem Vakif University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* singleton pregnancy at term \>37 weeks of gestational age

Exclusion criteria

* history of previous cesarean section * history of previous uterine surgery * multiple gestation, placenta previa, polyhydramnious, fetal macrosomia * uterine atony history * gestational diabetes mellitus, gestational hypertension, preeclampsia, current or previous history of heart disease, liver, renal disorders or known coagulopath * active labor (with regular uterine contractions and cervical dilatation \>4 cm

Design outcomes

Primary

MeasureTime frameDescription
The healing ratio6 monthsSix months after the operation, the integrity of the cesarean scar at the uterine incision site will be assessed by hydrosonography. The healing ratio will be calculated as the thickness of the residual myometrium covering the defect, divided by the sum of the thickness of the residual myometrium covering the defect and the height of the wedge-shaped defect.

Secondary

MeasureTime frameDescription
blood loss24 hoursThe hemoglobin and hematocrit values will be measured 24 hours after CS
additional sutures2 hoursnumber of additional hemostatic sutures

Countries

Turkey (Türkiye)

Outcome results

None listed

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