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Cesarean Section clinical trials

View clinical trials related to Cesarean Section.

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NCT ID: NCT02692729 Completed - Cesarean Section Clinical Trials

Transverse Supraumbilical Versus Pfannenstiel Incision for Cesarean Section in Morbidly Obese Women

Start date: March 2016
Phase: N/A
Study type: Interventional

This study aims to evaluate the efficacy and safety of transverse supraumbilical incision over Pfannenstiel incision in performing cesarean section for morbid obese pregnant women.

NCT ID: NCT02609217 Active, not recruiting - Cesarean Section Clinical Trials

Parents' Expectations and Experiences Around Cesarean Section in Belgium

Start date: November 2015
Phase: N/A
Study type: Observational

The aim of this study is to gain insight in the experiences and expectations of Belgian parents concerning primary cesarean section. This will be achieved by structured patient interviews and questionnaires in 24 women undergoing the procedure and their partners. This group will be divided into two subgroups of 12 multiparous and 12 nulliparous women and their partners.

NCT ID: NCT02577432 Completed - Cesarean Section Clinical Trials

Two Syringe Spinal Anesthesia Technique for Cesarean Section: A Simple Way to Achieve More Satisfactory Block and Less Hypotension

Start date: May 2013
Phase: N/A
Study type: Interventional

Background: Poor spinal anaesthesia block is common and is difficult to manage; so a technique to minimize its incidence is advisable. Hypotension is the commonest problem with spinal anesthesia. Multiple trials to prevent or combat hypotension using positional changes, fluid therapy and the use of vasopressors were tried. However, the drug choice and mode of administration as either bolus or infusion is still a matter of debate. Objectives: To compare the outcome of spinal injection of hyperbaric bupivacaine and fentanyl separately to standard injection of mixed fentanyl with hyperbaric bupivacaine. Design: A randomized, controlled clinical trial. Setting: Single medical center from 5/2013 to 10/2014. Patients & Methods: 124 parturient scheduled for elective cesarean section (CS) were randomly allocated into two groups, each 62 parturient: Group M received spinal anesthesia using 10 mg bupivacaine 0.5% premixed with 25 µg fentanyl in the same syringe and Group S received 25 µg fentanyl in one syringe and 10 mg bupivacaine 0.5% without barbotage in a second syringe. Intravenous fluid co-load with 15 ml/kg warm lactated ringer solution was started as fast drip during, and continued after spinal anesthesia. Patients were monitored for hemodynamic parameters, time of sensory onset and height of maximum sensory block, lower limb motor blockade was scored using modified Bromage scale and the frequency of side effects.

NCT ID: NCT02531828 Completed - Surgery Clinical Trials

Study Comparing the Polyurethane Films and Sugarcane Biopolymer Used as Dressings

Start date: August 2014
Phase: Phase 3
Study type: Interventional

The aim of this study is validate the use of biopolymer from sugar cane molasses film (POLYSHAFT®) a product developed in Experimental Station research laboratories (UFRPE) comparing to polyurethane film, or similar, used as a bandage after surgical correction of hypospadias, as well as other procedures. The main objective of the study is to prove the hypothesis the POLYSHAFT® presents similar or better outcomes in terms of biocompatibility, when compared to the polyurethane film when used as a bandage.

NCT ID: NCT02472327 Completed - Cesarean Section Clinical Trials

Decreasing Patient Dissatisfaction With Unplanned Cesarean Sections

Start date: June 2015
Phase: N/A
Study type: Interventional

Patient satisfaction after an unplanned cesarean section was studied and in the previous study it was noted that there were common themes that lead to patient dissatisfaction. The four common themes were: lack of trust regarding the indications for surgery, communication issues, loss of control, and fear during the situation. The purpose of this second phase of this study is to try and improve patient dissatisfaction by offering additional emotional support prior to the c/s with the hope of decreasing the trust issues toward physicians, decreasing the communication barriers, and decreasing the fear and loss of control. The additional emotional support that will be received prior to the cesarean section will be scripted based upon the findings of the investigators' prior study - the patient will be asked four questions and each question addresses the four themes that were noted in the previous study.

NCT ID: NCT02466776 Completed - Cesarean Section Clinical Trials

Comparison of Staples Versus Subcuticular Suture in Class III Obese Women Undergoing Cesarean Delivery

Start date: June 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the optimal skin closure technique (staples versus subcuticular suture) at the time of cesarean delivery in Class III obese women with body mass index (BMI) of >/= 40kg/m2.

NCT ID: NCT02464917 Completed - Cesarean Section Clinical Trials

Supplemental Oxygen Study

SOS
Start date: June 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare umbilical cord gases in subjects receiving oxygen at 10L/min via simple facemask to subjects receiving room air in those presenting for scheduled cesarean sections.

NCT ID: NCT02418026 Completed - Pain Clinical Trials

Improving Cesarean Section Experience Through Hypnotherapy

Start date: February 2013
Phase: N/A
Study type: Interventional

Cesarean section rates continue to increase worldwide, particularly in middle- and high-income countries. In France, the rate has now stabilized around 20 %. Cesarean section is a particular way of giving birth, sometimes desired, but sometimes feared. If some women do not feel affected by this way of giving birth, it is more difficult for others to live with. In this way, not being able to give birth trough natural way may be disturbing in motherhood. At La Rochelle hospital, more than 230 healthcare providers have been trained according to Erickson's hypnosis methodology. Among them, 40 are part of the anesthesia department and a committee oversees the hypnotherapist activities in pain management. The objective of the present study is to assess the benefit of hypnosis session for improving experience and reducing anxiety in women giving birth through surgery.

NCT ID: NCT02416310 Completed - Cesarean Section Clinical Trials

Transcutaneous Electrical Acupoint Stimulation on Gastrointestinal Function After Cesarean Section

TEAS
Start date: September 1, 2015
Phase: N/A
Study type: Interventional

To determine whether treating by transcutaneous electrical acupoint stimulation (TEAS) during perioperative could alleviate the postoperative gastrointestinal complications after cesarean section under combined spinal epidural anesthesia compared with control and non-acupoint group.

NCT ID: NCT02380898 Completed - Cesarean Section Clinical Trials

Preemptive Ketorolac for Shoulder Tip Pain During Cesarean Section

Start date: March 2015
Phase: Phase 4
Study type: Interventional

Our study is planned to investigate if pre-emptive Ketorolac would decrease the incidence of intraoperative shoulder tip pain and improve discomfort during Caesarean section.