Comparison of the outcomes of suture technique with suture fluid adhesion and routine cesarean section

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20130812014333N134

Enrollment

Registered

2019-12-26

Start date

2020-01-10

Completion date

Unknown

Last updated

2020-01-13

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

Conditions

cesarean. Infection of obstetric surgical wound

Interventions

Intervention 1: In the intervention group after the cesarean section, EPIGLU suture adhesive that made in Germany will be used. Intervention 2: In the control group, sutures are used as usual.

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years gestational age greater than or equal to 24 weeks termination of pregnancy with an elective or emergency cesarean section

Exclusion criteria

Exclusion criteria: BMI> 30 pregnancy with dead fetus drug abuse fetal macrosomia prolonged runoff and coagulopathy

Design outcomes

Primary

Measure	Time frame
Intensity of pain. Timepoint: End of study. Method of measurement: Asking the patient.;Wound infection. Timepoint: End of study. Method of measurement: Doctor observation.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHoda Alsharif

Kermanshah University of Medical Sciences

hodaalsharif@yahoo.com+98 83 3427 6306

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026