Caesarean deliveries Pregnancy and Childbirth Single delivery by caesarean section
Conditions
Interventions
This trial is taking place at the Istanbul Dr. Lutfi Kirdar Kartal Research and Training Hospital, Department of Obstetrics and Gynaecology. Approximately 180 patients will be recruited, 90 patients i
Sponsors
Dr. Lutfi Kirdar Kartal Research and Training Hospital (Turkey)
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Pregnancies greater than 34 weeks of gestation 2. Women between ages of 18 - 45 years 3. First time caesarean section
Exclusion criteria
Exclusion criteria: 1. Previous lower abdominal incision 2. Pregnancies less than 34 weeks of gestation 3. Known severe anaemia 4. Bleeding disorders 5. Intrapartum febrile illness
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Operation time 2. Time until delivery of neonate 3. APGAR score 4. Blood loss 5. Operative complications 6. Number of used sutures All measured intra-operatively. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Length of hospital stay 2. Wound seroma 3. Wound infection 4. Mobilisation time 5. Visual Analogue Scale score at 6 and 24 hours of the operation 6. Time of bowel restitution Measured post-operatively at 6 hours, 24 hours and 5 days. | — |
Countries
Turkey
Outcome results
None listed