Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT06005831 |
| Other study ID # |
2020/14-02 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
January 1, 2021 |
| Est. completion date |
December 31, 2021 |
Study information
| Verified date |
August 2023 |
| Source |
Firat University |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
Uterine compression methods reduce the amount of postpartum bleeding. In our study, we
investigated the effect of fundal pressure, which will be created by a sandbag placed on the
abdomen, on reducing post-cesarean bleeding. Material and Methods: A total of 482 patients
who delivered by cesarean section (CS) in the Obstetrics Clinic of Fırat University Faculty
of Medicine between January 2021 and December 2021 were included in this prospective,
randomized, single-center study.
Description:
A total of 482 patients who gave birth by CS in the Obstetrics Clinic of Fırat University
Faculty of Medicine between 1 January 2021 and 31 December 2021 were included in the study.
Approval was obtained from the Ethics Committee of Fırat University for this prospective
randomized single-center study (Ethics committee date = 15.10.2020; decision no =
2020/14-02). The 482 patients who had CS were divided into two groups, control group (n =
246), weighted group (n = 236) was randomized. Each patient was followed up in our obstetrics
clinic until discharge from the hospital after surgery and the data were analyzed. The same
techniques were used in all surgical procedures in order not to create differences in terms
of surgical techniques and operation times that may affect intraoperative bleeding. However,
to minimize inter-operator variations, surgical procedures were performed by operators with
sufficient surgical experience.
The standard sandbag used in our clinic was 20 × 20 × 3 cm3 in dimensions and 3 kg in weight.
Sandbags of the same standard were used for all patients. After the patient was taken to the
patient's bed, the uterine fundus was palpated, and then the sandbag was placed on the
abdomen, just above the fundus, in such a way as to apply pressure to the fundus. The sandbag
was kept on the abdomen for approximately 6 hours. During this period, the patient was
followed up frequently and care was taken not to change the position of the sandbag. Sandbags
were removed just before our patients were mobilized (approximately 6 hours). The sandbag was
placed on the same spot in each patient by the obstetric assistants in our author team. In
addition, preoperative and postoperative follow-ups and data acquisition and storage were
performed by the same team 2.1 Study Design
It is a prospective, randomized, controlled single-center study.
2.2 Inclusion Criteria
All cases with CS who had a live pregnancy after 24 weeks of gestation were included in the
study.
2.3 Exclusion Criteria
- Invasion anomaly,
- Diagnosed with preeclampsia,
- Placenta previa cases,
- Hypertensive pregnant women receiving antihypertensive therapy,
- Diabetic pregnant women,
- Multiple pregnancies,
- Major hepatic, cardiac, renal, respiratory disorders
- Deep vein thrombosis during pregnancy,
- Receiving anticoagulant therapy
- Patients who developed atony and uterine rupture in the operating room,
- Suspected placental invasion
- Uterine balloon tamponade
- Arterial embolization
- Uterine and hypogastric artery ligation,
- Uterine compression sutures
- Intraoperative blood loss was estimated to be over 1000 mL during CS and who received
intraoperative blood transfusion
2.4 Patient Selection
For randomization, patients were fully informed about the study while preparing for CS.
Sandbags were placed in all cases included in the study after meeting the study criteria for
between 1 January 2021 and 30 June 2021. Sandbags were not placed in the cases who met the
study criteria and were included in the study between 1 July 2021 and 31 December 2021.2.5
Sampling Technique
Qualified participants who gave informed consent to participate in the study were randomly
assigned to groups. Visual analog scale (VAS) was used for postoperative pain scoring at the
8th and 24th postoperative hours. The patient included in the study was randomized into
control group or weighted group by another assistant doctor who did not participate in the CS
and did not know about the patient.
2.6 Postoperative Monitoring
All cases were given 10 IU of oxytocin IV during CS, after prophylactic antibiotic therapy
and placenta separation. After CS, 40 IU of oxytocin (Synpitan® forte ampule 5 IU, Deva,
Istanbul, Turkey) was administered intravenously in 500 mL saline and at an infusion rate of
125 mL/hour. At the same time, 0.2-0.4 µg methylergonovine maleate (Methergine® ampule 0.2
µmg, Sandoz, Istanbul, Turkey) was given intravenously/intramuscularly in cases without
hypertension. All patients were treated according to the postoperative protocol for CS
performed in our obstetrics clinic. At the 8th and 24th hours postoperatively, the
researchers determined the patient's hemoglobin (Hb) and hematocrit (Hct) concentrations and
the amount of vaginal bleeding. In addition, the time of milk coming from the breast and VAS
were performed. Patients with a postoperative Hb value of <7 g/dL received blood transfusion.
Considering the risks of blood transfusion, blood transfusion is primarily planned in
symptomatic patients with an Hct value of <20%, as stated in the bulletin of The American
College of Obstetricians and Gynecologists (ACOG), but if the Hb is below 7 g/dL, it is
hemodynamically stable and in asymptomatic patients, the treatment is individualized and
alternative to transfusion, oral anti anemic or intravenous iron therapy is applied.
2.7 Determination of the Amount of Postoperative Blood Loss
Postoperative blood loss was determined by monitoring the pad and measuring the hemoglobin
values at the 8th and 24th hours in all cases. Standard pads measuring 10 × 10 cm2 was used.
The main advantage of this method of visually assessing blood loss is that it is a real-time
assessment and allows the person accompanying the delivery to correlate it with the patient's
clinical findings. However, significant differences between clinical evaluation and actual
measurements have been clearly demonstrated in many studies has been reported that
gravimetric blood loss estimation methods or serum lactate measurements can provide a more
objective assessment of bleeding. It has been reported that visual and gravimetric blood loss
estimation measurements show a high degree of bias and therefore their routine use cannot be
recommended. On the other hand, it has been stated that colorimetric technology offers
real-time measurement and has a high degree of correlation. For this reason, we used the
preoperatively and postoperatively at the 8th and 24th hours hemoglobin values. Postpartum
anemia was defined as hemoglobin concentration (Hb) <10 g/dL in the postpartum period.
