Clinical Trials Logo

Cesarean Delivery clinical trials

View clinical trials related to Cesarean Delivery.

Filter by:

NCT ID: NCT01216410 Completed - Cesarean Delivery Clinical Trials

Prevention of Intraoperative Nausea and Vomiting During Cesarean Section

Start date: December 2008
Phase: N/A
Study type: Interventional

The study investigates the incidence of intraoperative nausea and vomiting under spinal anesthesia using a phenylephrine infusion with and without prophylactic antiemetics.

NCT ID: NCT00985764 Completed - Clinical trials for Cesarean Delivery With Placental Previa

Venous Air Embolism in Cesarean Delivery, Especially Placental Previa

Start date: May 2007
Phase: N/A
Study type: Observational

Effects of placenta previa on incidence and severity of venous air embolism in patients during cesarean delivery

NCT ID: NCT00957593 Completed - Cesarean Delivery Clinical Trials

Induction of Labor With Oxytocin: When Should Oxytocin be Held?

Start date: February 2009
Phase: N/A
Study type: Interventional

The investigators propose to perform a prospective randomized control trial to compare the rate of cesarean delivery in women where Oxytocin (OT) is discontinued once active labor begins (5 cm dilation) when compared with women where OT is continued at a maintenance level per the usual protocol. One study group will follow an oxytocin protocol which is incremental until 5 cm dilation and then maintained at the same level throughout labor. The second arm will follow an oxytocin protocol also incremental, but then discontinued once the cervix is 5 cm. The primary outcome will be the rate of cesarean delivery between the groups. Secondary outcomes to be evaluated will include duration of the labor, fetal heart rate abnormalities, and frequency of uterine hyperstimulation, maternal and neonatal outcomes. As mentioned in the study proposal, the proposed experimental arm is currently not performed as part of the oxytocin guidelines at the investigators' institution. One study from Israel suggests no difference in pregnancy outcomes with the proposed use of oxytocin. Although some providers stop the oxytocin in active labor for their patients, this is not a commonly performed procedure at the investigators' institution. The investigators are not aware of other institutions employing the above practice.

NCT ID: NCT00884026 Completed - Hypotension Clinical Trials

Can Augmentation Index (AIx) be Used to Predict Hypotension After Spinal Anesthesia?

Start date: March 2009
Phase: N/A
Study type: Interventional

A fall in blood pressure (hypotension) occurs in one third of spinal anesthetics administered to pregnant patients undergoing cesarean delivery. However, predicting which patients will experience hypotension following spinal anesthesia has proven difficult. Pulse wave analysis is a repeatable and reproducible method for investigation of cardiovascular function. A device called a SphygmacorTM can be used to measure pulse. The pulse measurement is called the Augmentation Index (AIx). AIx has been useful in detecting risks associated with blood pressure changes after complex surgery in patients with heart and blood vessel disease. In this study the investigators wish to see if it is possible to predict if a subject will experience hypotension based on her AIx measurement preoperatively.

NCT ID: NCT00815022 Completed - Cesarean Delivery Clinical Trials

Influence of Anesthetic Temperature on Cephalad Sensory Blockade With Spinal Anesthesia

ATOCEB
Start date: December 2008
Phase: N/A
Study type: Interventional

Several factors influence the extension of anesthetic mixture during spinal anesthesia including anesthetic gravity, body position, drug volume, and drug-delivering velocity. However, the effect of temperature of anesthetic mixture on the cephalad sensory blockade is hitherto unknown. The investigators hypothesized that different temperatures of the anesthetic mixture had different velocity of extension after spinal anesthesia. In addition, previous studies suggest that parturients have relative higher sensitivity to temperature. Herein the investigators proposed that the temperature of anesthetic mixture had more extensive effect on the cephalad sensory blockade with spinal anesthesia for cesarean delivery.

NCT ID: NCT00799955 Completed - Cesarean Delivery Clinical Trials

Comparing 2 Types of Pain Relief After Cesarean Delivery: Spinal Morphine and TAP Block

Start date: October 2008
Phase: N/A
Study type: Interventional

Summary Brief Summary Standard care for pain relief after cesarean delivery is spinal morphine. Spinal morphine may be unsuitable for patients having general anesthetic or prior morphine-related side effects and can be less effective in patients with morphine tolerance. An alternative is a TAP block where local anesthetic is deposited between the abdominal muscles consequently numbing the area and providing pain relief. The investigators believe a TAP block will provide equivalent pain relief to spinal morphine.

NCT ID: NCT00736580 Completed - Cesarean Delivery Clinical Trials

Glove Perforation When Using Blunt Verses Sharp Needles in Cesarean Delivery

Start date: June 2008
Phase: N/A
Study type: Interventional

This study is assessing whether there is a decrease in surgical glove punctures using blunt tipped needles compared with sharp needles for suturing during Cesarean Delivery.

NCT ID: NCT00616174 Completed - Cesarean Delivery Clinical Trials

Does Warming Mothers During Cesarean Delivery Help Keep Babies Warm When Delivered?

Start date: February 2008
Phase: N/A
Study type: Interventional

The purpose of this study to investigate whether using a special warming blanket during Cesarean delivery helps maintain a normal body temperature in the baby when compared to mothers that are not warmed (standard care at BC Women's Hospital). Doctors observed that some babies have low body temperatures when they are born by Cesarean delivery. Since baby temperatures are dependant on the temperatures of their mothers, we believe that keeping the mother warm during surgery with the use of a special warming blanket that is filled with warm air will result in the baby being warmer at birth.

NCT ID: NCT00371722 Completed - Cesarean Delivery Clinical Trials

Appendectomy Versus no Appendectomy With Cesarean Section

Start date: July 2002
Phase: N/A
Study type: Interventional

Women having cesarean section will be divided into two groups - cesarean section alone or cesarean section with appendectomy. The purpose is to see if the appendectomy can be done without adding any complications to the maternal post-operative course. The hypothesis is that there is no increased incidence of wound infection, post-operative morbidity or longer hospital stay associated with elective appendectomy at the time of Cesarean Section.