Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04734366 |
Other study ID # |
GaziosmanpasaKHD |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
December 17, 2020 |
Est. completion date |
July 15, 2021 |
Study information
Verified date |
February 2023 |
Source |
Tokat Gaziosmanpasa University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Cesarean delivery rates in Turkey as well as all over the world are increasing. Recent data
in Turkey shows that the value of cesarean delivery rate reached 53%. This worldwide increase
causes new concerns. Incomplete healing of the uterine scar after cesarean is a complication
with potential long-term consequences. There is evidence that the risk of uterine scar
defects is associated with the number of previous cesarean deliveries and the method of
uterotomy closure. Study was designed as prospective randomized clinical trial to analyze the
effects of two different uterine suture techniques. The investigators aim is to compare the
closure of the incision with the "baseball" suture technique and the single-layer locking
technique in terms of the incidence and depth of the isthmocele in the uterine incision scar
as a short-term result.
Description:
This study was designed as a double-blind randomized prospective and cross-sectional.
Cesarean delivery planned patients who will admit to the Obstetrics and Gynecology Clinic,
Tokat Gaziosmanpasa University Research and Application Center between January 2021 and June
2021 will be evaluated. Participation of the patients in the study will be based on written
consents. All patients who meet the inclusion criteria will be randomized into two groups
(i.e., "baseball" or single layer locked).
This study was approved by Tokat Gaziosmanpasa University Institutional Review Board and
Ethics Committee (Project no= 20-KAEK-311, Approval Date= 12/17/2020).
Pregnant women who are over 37 weeks, have no pregnancy complications, and will undergo
uterine surgery for the first time will be included in the study. Exclusion criteria are
determined as: Preoperative hemogram value below 10mg/dL, active labor (regular contraction
and> 4cm cervical opening), placental anomaly, previous uterine surgery, chorioamnionitis,
premature rupture of membranes, additional disease, body mass index BMI> 35kg / m2, consuming
tobacco and / or alcohol, needing blood transfusion and multiple pregnancy.
Randomization will be created on a computer controlled by a statistician to create two
groups. Before cesarean delivery, sealed, opaque and numbered envelope containing the
definition and image of the suture technique will be reported to the surgeon. Participants
included in the study 3 months after the operation will be called for control by an external
observer. Follow-up data and ultrasound measurements of uterine incision scar area will be
documented by sonographer who does not know the uterotomy closure technique applied to the
patient.
During the follow up examination, weight and breastfeeding status of the patient and
ultrasound measurement of uterine length, uterine position, residual myometrial thickness,
isthmocele depth, isthmocele width, cervical thickness, isthmocele fundus distance,
isthmocele cervical distance, hypoechoic isthmocele width in transverse plane will be
recorded.
The sample size was calculated based on a study by Roberge S et al. (2016) titled Impact of
uterine closure on residual myometrial thickness after cesarean: a randomized controlled
trial. The mean residual myometrial thickness values of this study were found to be 3.8 ±
1.57 in the single-layered group and 4.77 ± 1.34 in the double-stitched group. The power
analysis performed using GPower 3.1 (http://www.gpower.hhu.de/) program, when 80% power and
alpha = 0.05 are taken, the total sample size calculated using the student's t test was found
to be 36 for each group. Considering possible problems, it is planned to include 80
participants, 40 for each group. The normal distribution of the data of the measurements will
be analyzed with the Kolmogorov-Smirnov test. The data of two groups of patients will be
analyzed with the Statistical Package for Social Sciences (SPSS) version 20 program using
one-way ANOVA analysis, post-hoc test, T-test, chi-square and Fisher test according to the
data characteristics. Statistical significance will be accepted as p <0.05.