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Cesarean Section Complications clinical trials

View clinical trials related to Cesarean Section Complications.

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NCT ID: NCT05458518 Recruiting - Clinical trials for Cesarean Section Complications

Caesarean Wound Dressing Removal Study

Cesarean
Start date: July 1, 2022
Phase: N/A
Study type: Interventional

An open labelled randomised trial on the timing of wound dressing removal for emergency caesarean delivery in labour.

NCT ID: NCT05427149 Completed - Clinical trials for Cesarean Section Complications

The Effect of Intrathecal Magnesium Sulfate on Shivering

Start date: May 10, 2022
Phase: N/A
Study type: Interventional

Shivering after spinal anesthesia is a common complication. Mangesium sulfate, which can be used intrathecally, is effective in preventing tremor. But what is the ideal dose?

NCT ID: NCT05396430 Enrolling by invitation - Clinical trials for Cesarean Section Complications

Duration of Urinary Catheter Treatment After Cesarean Delivery Under Spinal Anesthesia

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

In this study a total of 150 parturients undergoing cesarean delivery under spinal anesthesia will be randomized to have their urinary catheters kept in place for 8, 10 or 12 hours. The incidence of urinary retention and interventions needed for any potential urinary retention will be assessed.

NCT ID: NCT05396417 Enrolling by invitation - Clinical trials for Cesarean Section Complications

How Well do the Current Cesarean Deliveries Adhere to the Published ERAS Guidelines?

Start date: January 1, 2023
Phase:
Study type: Observational [Patient Registry]

Local guidelines for the postoperative care of women who have undergone cesarean delivery at the HUS/Women's hospital are based recommendations by the ERAS society. This study will take a prospective sample of 500 parturients who have gone through a cesarean delivery and their care will be verified against the local check-list for cesarean delivery.

NCT ID: NCT05396378 Not yet recruiting - Clinical trials for Gestational Diabetes

Early Recovery After Cesarean Delivery - Maternal Glucose Homeostasis Following Preoperative Glucose Dose

Start date: July 1, 2023
Phase:
Study type: Observational

Diabetic parturients planned for cesarean delivery will be recruited for the study. They will receive a fixed glucose dose to mimize the effects of fasting preoperatively and their blood glucose levels will be monitored.

NCT ID: NCT05395585 Completed - Clinical trials for Cesarean Section Complications

The Effect of Placental Spontaneous Delivery Versus Manual Removal on Blood Loss During Cesarean Section. A Comparative Study

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

The mode of placental delivery may contribute to an increase or decrease in the morbidity associated with CS, and many studies have shown it to be a key role in determining the blood loss during CS. Manual removal of the placenta has been implicated in increased blood loss during CS. However, other researchers concluded that it had no detrimental effect on blood loss

NCT ID: NCT05391685 Not yet recruiting - Clinical trials for Cesarean Section Complications

EFFECT OF SCAR RELEASE TECHNIQUES ON CHRONIC SCAR PAIN AND MOBILITY POST CESAREAN SECTION

Start date: June 20, 2022
Phase: N/A
Study type: Interventional

Purpose of the study: The aim of this study is to determine the effect of scar release techniques on chronic scar pain and mobility post cesarean section. Hypothesis: - H0: There is no effect of scar release techniques on chronic scar pain and mobility post cesarean section. - HA: There is effect of scar release techniques on chronic scar pain and mobility post cesarean section.

NCT ID: NCT05385276 Recruiting - Clinical trials for Cesarean Section Complications

Transverse Supraumbilical Versus Pfannenstiel Incision For Cesarean Section In Morbidly Obese Women

Start date: May 1, 2021
Phase: N/A
Study type: Interventional

cesarean section is one of the most common operative procedures performed in modern obstetrics, that become increasingly common in both developed and developing countries for a variety of reasons today, thus any useful refinement in the operative technique, however minimal, is likely to yield substantial benefits. In morbidly obese women with a panniculus, the supraumbilical incision is a new technique that showed definite advantages over the Pfannenstiel incision that will avoid burying the wound under a large panniculus and affords excellent abdominal exposure, less blood loss, less post-operative pain, earlier ambulation, and shorter hospital stay. All these advantages were attributed to minimal tissue manipulation.

NCT ID: NCT05382624 Completed - Hypotension Clinical Trials

The Relationship Between Abdominal Circumference: Hip Ratio and Ephedrine Requirement

Start date: April 1, 2020
Phase:
Study type: Observational [Patient Registry]

This prospective observational study aimed to investigate whether there is a relationship between weight, height, BMI, abdominal circumference (AC), hip circumference (HC), and AC-to-hip ratio with the incidence of hypotension in patients undergoing cesarean section under spinal anesthesia.

NCT ID: NCT05380531 Recruiting - Opioid Use Clinical Trials

Personalized Perioperative Analgesia Platform (PPAP) for Cesarean Section

PPAP C-Section
Start date: December 5, 2022
Phase: N/A
Study type: Interventional

The purpose of this collaborative CTSA (Clinical and Translational Science Award) application is to develop an innovative perioperative precision analgesia platform (PPAP) to improve analgesia and reduce serious immediate and long-term adverse outcomes of perioperative opioids in breastfeeding mothers and their infants