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Cesarean clinical trials

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NCT ID: NCT05133271 Recruiting - Spinal Anesthesia Clinical Trials

Prediction of Maternal Arterial Hypotension After Spinal Anesthesia by Passive Leg Raise Test.

EDLIDL
Start date: February 3, 2021
Phase: N/A
Study type: Interventional

Spinal anesthesia for cesarean section is associated with a high incidence of low blood pressure. However, the pathophysiology of this arterial hypotension is not unequivocal and could involve, in addition to drug vasoplegia, a mechanical cause linked to lower caval compression or even true or relative hypovolemia. Passive leg raise test has been proposed in an attempt to identify parturients who are more likely to develop low blood pressure after spinal anesthesia. Nevertheless, the data available on this volume expansion test to predict hemodynamic variations after performing spinal anesthesia are still limited and few objective criteria have been described to predict this arterial hypotension. The objective of the research is to study the hypothesis according to which the presence of hypovolaemia (true or relative) objectified by a positive passive leg raise test would cause hypotension more frequent and more marked in intensity.

NCT ID: NCT04876547 Completed - Appendicitis Acute Clinical Trials

Are Cesarean Section and Appendectomy in Pregnancy and Puerperium Interrelated?

APPENDECTOMY
Start date: January 1, 2015
Phase:
Study type: Observational

It is not known whether appendectomy for acute appendicitis (AA) increases the Cesarean section (CS) rate and whether CS increases the likelihood of AA and appendectomy in the early puerperium. In this study, delivery type and delivery outcomes and appendectomy during pregnancy and puerperium were analyzed.

NCT ID: NCT04599842 Completed - Clinical trials for Ceserean Section and Postoperative Pain

Analgesic Effect of Erector Spinae Plane Block After Caesarean Section

AnESPaCS
Start date: March 15, 2020
Phase: N/A
Study type: Interventional

Background: Our hypothesis was that bilateral ESP block applied from the transverse process of T9 in women who underwent elective cesarean section with pfannenstiel incision under spinal anesthesia could provide effective postoperative analgesia.The primary outcome in this study was total opioid consumption for 24 hours. Material and Method: This randomized prospective study was carried out on 50 pregnant women who was scheduled for elective cesarean delivery via a Pfannenstiel incision with spinal anesthesia.Patients were randomly allocated in to two equal groups.Group SA was categorized as the group which spinal anaesthesia alone (SA) was performed, Group SA+ESP was categorized as group which SA+ESP block was performed. All groups received 7 mg isobaric bupivacaine +15 µg fentanyl intrathecally through spinal anesthesia. The SA+ESP group, ESP block was performed at the ninth thoracic transverse process with 20 ml 0.25% bupivacaine + 2 mg dexamethasone immediately after the operation. Total fentanyl consumption in 24 hrs, visual analogue scale (VAS) score for pain, time to the first analgesic request were evaluated postoperatively.

NCT ID: NCT03915847 Completed - Clinical trials for Cesarean, Residual Myometrial Thickness

Evaluation of Cesarean Scar After Three Different Uterine Closure Technis

Start date: April 16, 2019
Phase: N/A
Study type: Interventional

The study compares three techniques of uterine closure on myometrium thickness at the site of uterine scar of women who underwent repeated cesarean section. Cesarean scar will be evaluated by transvaginal ultrasound six months after cesarean.

NCT ID: NCT03719625 Not yet recruiting - Cesarean Clinical Trials

Norepinephrine Versus Ephedrin for Prevention of Post Spinal Anesthesia in Cesarean Section

Start date: January 2, 2019
Phase: Phase 4
Study type: Interventional

Spinal anesthesia is still the gold standard anesthetic method for elective and urgent cesarean section, the post spinal hypotension remains the most frequent complication of this procedure and is still responsible of considerable maternel and fetal morbidity. It is recommanded to prevent this post spinal hypotension with fluid coloading and prophylactic vasopressors administration. The aim of this study is to compare the efficency and the safety of norepinephrin and ephedrin prophylactic administration to reduce the incidence of post spinal hypotension in cesarean section.

NCT ID: NCT03672071 Recruiting - Cesarean Clinical Trials

Effects of Norepinephrine-ephedrine Combination on Maternal Hemodynamics

Start date: September 30, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effect of combined use of Ephedrine and Norepinephrine on maternal hemodynamics in patients undergoing cesarean delivery under spinal anesthesia. Secondary aim of the study is to investigate the effect of this combination on neonatal Apgar score and umbilical cord blood gas values.

NCT ID: NCT03644433 Recruiting - Clinical trials for Cesarean Section Complications

Impact of Uterine Closure Techniques on the Cesarean Scar Thickness After Repeated Cesarean Section

Start date: August 23, 2018
Phase: N/A
Study type: Interventional

We compares two techniques of uterine closure on myometrium thickness at the site of uterine scar of women who underwent repeated cesarean section. We will evaluate myometrial thickness by transvaginal ultrasound six months after cesarean.

NCT ID: NCT03544710 Completed - Clinical trials for Cesarean Wound Disruption With Postnatal Complication

Impact of Preoperative Bathing on Post Caesarean Section Surgical Site Infection

SSI-MUST
Start date: December 7, 2017
Phase: N/A
Study type: Interventional

Surgical site infection (SSI) is the commonest hospital-acquired infection globally, and prevalence is much higher in the low-income countries. Caesarean delivery carries a 5-20 fold risk for developing postpartum sepsis. SSIs cause significant morbidity, prolonged hospitalization and mortality. Simple and inexpensive interventions like preoperative bathing need to be studied, to assess their impact on surgical site infection rates.

NCT ID: NCT03433976 Recruiting - Cesarean Clinical Trials

Prilocaine or Bupivacaine for Spinal Anesthesiain Pregnant

Césarcaïne
Start date: May 7, 2018
Phase: Phase 2
Study type: Interventional

The planned cesarean section is an intervention with a standard operating time of less than 40 minutes in trained teams. Hyperbaric Bupivacaine is the local anesthetic (LA) reference for these operations. But the duration of its motor block is generally greater than 3 hours. The purpose of this study is to show a reduction in motor block time with hyperbaric Prilocaine by at least 30 minutes, which would allow mothers and their children to return to the maternity ward earlier and thus improve the circulation of patients within the maternity's PACU.

NCT ID: NCT03147781 Completed - Lactation Clinical Trials

Auricular Therapy for Postpartum Lactation

Start date: April 7, 2017
Phase: N/A
Study type: Interventional

The aim of this study is to function as a pilot study in evaluating the effects of auricular therapy (AT) on lactation for women in the immediate post cesarean period while examining the feasibility of the three-parallel-arm, sham-controlled randomized design. The study hypothesizes that post cesarean women who receive AT with standard care for 96 hours postpartum have earlier onset of lactogenesis II and larger milk production when compared with women who receive sham AT with standard care or standard care alone.