Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT04681378 |
Other study ID # |
ID: 7-2016OBSGN17 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
January 1, 2017 |
Est. completion date |
July 1, 2020 |
Study information
Verified date |
December 2020 |
Source |
Menoufia University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
The purpose of this study was to compare the short term operative outcomes of three different
surgical techniques for uterine incision closure during cesarean section (CS).
This trial enrolled 120 patients scheduled for primary cesarean delivery. Patients were
randomized into either classical double layer uterine closure, purse string double layer
uterine closure (Turan), or our new approach of uterine closure (double layer step up-step
down technique). For short term comparison, transvaginal ultrasonography was planned for all
patients 6 weeks after surgery. Compared to group II and Group III, residual myometrial
thickness was significantly thinner in group I (P< 0.001). The number of patients with
uterine niche was 10 (50% of all scar defects) in group I whereas it was 4 (20%) in group II
and 6 (30%) in group III. Operative time was significantly longer in group II (P< 0.001).
This led to our conclusion that Turan technique and our new approach are associated with
thicker myometrial thickness and less frequency of uterine scar defect than classical double
layer uterine incision closure; however, our approach takes less operative time.
Description:
The investigators performed single site randomized clinical trial that was conducted at
department of Obstetrics and Gynecology, Menoufia University Hospital, which is a large
tertiary center in the Delta region in Egypt. The study population consisted of 120 eligible
pregnant women with a singleton first-time cesarean delivery without preterm rupture of
membranes, contractions or cervical dilatations that were recruited from the inward section
one day before surgery from January 2017 to April 2019; only 114 cases remained for analysis.
The study was approved by our hospital ethics committee and a written consent was obtained
from each participant woman after full explanation of the study design. No important changes
occurred to the trial design after it began, and the CONSORT guidelines was observed and
completed.
Exclusion criteria were: pregnant women who refused to participate, women under age of 18
years, history of previous CS or any other uterine surgery ( Hystrotomy , myomectomy,
perforation),placenta previa, abruptio placenta, fibroids located in the cervical or the
cervico-corporal border, presence of maternal disease ( diabetes mellitus, anemia, connective
tissue disorders, uterine malformations), reoperation following the CS, and presence of
chorioamnionits. Secondary exclusion criteria were the need for more than three additional
single sutures for hemostasis.
One author evaluated all obstetric patients who applied to the delivery room within the study
period and selected eligible cases. After excluding patients who did not meet the inclusion
criteria and patients who refused to participate, all remaining patients were equally
randomized into either classical double layer uterine closure (group I), purse string double
layer uterine closure (Turan technique, group II), or our technique of double layer step up-
step down uterine closure (group III).
A computer-generated random numerical table (Randomization Generator Version 1.0) was used by
our statistical department to prepare sealed opaque envelopes containing a group assignment.
Three groups of envelopes-corresponding to the study groups were given to an anesthesia
nurse. The nurse distributed envelopes to patients, alternating between groups during
preanesthetic consultation. The patients were blinded the groups, and two authors performed
the operations randomly. Another author who was blinded to the suturing technique performed
all of the ultrasonographic examinations at 6 week follow up visit.
All cesarean deliveries were performed under spinal anesthesia. An abdominal opening was made
through a slightly curved transverse incision that was placed 3-4 cm above the symphysis
pubis (Pfannestiel incision). The subcutaneous tissue was left untouched apart from midline.
The rectus sheath was separated along its fibers and the rectus muscles pulled apart.
Stretching with index fingers opened the peritoneum and the uterus was opened by transverse
lower segment incision (Kerr incision), then the hole was enlarged between the index finger
of one hand and the thumb of the other hand.
Classical double layer closure of uterine incision was performed as follows: a holding Vicryl
1-0 was placed in the in the left corner to stabilize and define the demarcation of the
suture line. A continuous unlocked stitch beginning at the right corner was used, closing the
whole thickness of the uterine wall, including the decidual layer. The second unlocked stitch
was performed by Vicryl 1-0 in a lateral -lateral (horizontal) position, adapting the first
layer. Up to three additional single sutures were added for hemostasis if required. The Turan
technique may be summarized as follows: beginning in one corner, the incision is closed using
Vicryl 1-0 stitch. The first layer is transversely passed through the inner
myometrium-decidua line, and second layer is transversely passed through outer
myometrium-visceral line continuously in the form of a purse string closure. With this
technique, the original string is returned to the starting point and tied with a knot.
Following the double layered purse-string closure, the aperture left in the middle of the
uterine incision is closed with one separate figure of eight suture (Figure 1A). Our new
approach can also be summarized as follows: the incision is closed using Vicryl 1-0 stitch
starting from one corner. The first layer is transversely passed through the inner
myometrium-decidua line, and second layer is transversely passed through outer
myometrium-visceral line continuously by alternating continuous stitches through the upper
(step up) and the lower (step down) uterine flaps. The original string is returned to the
starting point and tied with knot as in Turan technique. Following the double layered step
up-step down closure, additional single sutures were added for hemostasis if required (Figure
1B). Included in the surgical technique was uterine exteriorization. The visceral and
parietal layers were left open and the rectus muscle was not stitched. The rectus sheath was
stitched with a continuous unlocked no 1 Vicryl and subdermal was closed in all patients.
All patients received prophylactic intravenous antibiotics (Cefazolin sodium vial. 1gm, i.v)
preoperatively to reduce the rate of wound infection. In addition, uterotonics (5 IU units of
oxytocin) were given intravenously as a bolus, before manual removal of the placenta to
prevent postpartum hemorrhage. During the surgery, one author recorded operative time from
skin incision to skin closure, blood loss, type of uterine closure technique used, and Kerr
incision length before and after suturing and whether additional sutures for hemostasis were
needed.
All patients were discharged within 3 days of the operation and a detailed transvaginal
ultrasound examination was planned for all patients 6 weeks after surgery. Examinations were
performed with C8-4V endocavitary transducer with frequency of 4-8 MHz (Philips, HD11 XE
Ultrasound system, USA). The uterus was visualized in a sagittal plane with both the
endometrium and the cervical canal visible, the scar area was magnified and the outcome
measures were obtained from a frozen image. The scar was then visualized in a transverse
plane by carefully rotating the probe at the level of the scar. Our main variable for scar
evaluation was residual myometrial thickness (RMT). The cesarean scar site was identified as
a small triangular anechoic defect in the anterior wall of the uterus (uterine niche). In
these patients RMT was measured from the top of niche to serosal surface. In patients without
a scar defect RMT was measured from the delineation of the endometrium to the serosal surface
at the level of CS scar and total myometrial thickness was measured at the myometrium
adjacent to CS scar in all patients (Figure 2). If a scar defect was identified,
investigators measured in a sagittal plane its height (distance from the base/anterior lining
of the endometrium to the apex) and width (W) at its base. The length of the defect at its
base in a transverse axis (distance between the proximal and distal parts of the myometrium
of the anterior uterine wall) was also recorded.