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Cesarean Section clinical trials

View clinical trials related to Cesarean Section.

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NCT ID: NCT04432675 Completed - Cesarean Section Clinical Trials

Effects of Crystal Solution and Colloid Solution on Mother and Fetus

Start date: January 30, 2022
Phase: Phase 4
Study type: Interventional

Comparison of the effects of crystal solution (lactic acid Ringer's solution) and colloid solution (hydroxyethyl starch) on mother and fetus after cesarean section

NCT ID: NCT04399707 Recruiting - Analgesia Clinical Trials

Transcutaneous Electrical Nerve Stimulation for Post-Cesarean Pain Control

Start date: January 29, 2020
Phase: N/A
Study type: Interventional

Purpose of study is to evaluate the efficacy of transcutaneous electrical nerve stimulation (TENS) for post-operative pain control after a cesarean delivery compared to placebo and no TENS.

NCT ID: NCT04367103 Completed - Hypotension Clinical Trials

Norepinephrine for Hypotension in Cesarean Section

Start date: April 10, 2021
Phase: N/A
Study type: Interventional

Hypotension is a very common consequence of the sympathetic vasomotor block caused by spinal anesthesia for cesarean section. Maternal symptoms such as nausea, vomiting and dyspnea frequently accompany severe hypotension, and adverse effects on the fetus, including depressed APGAR scores and umbilical acidosis, have been correlated with severity and duration of hypotension. Because hypotension is frequent, vasopressors should be used routinely and preferably prophylactically.

NCT ID: NCT04360382 Completed - Cesarean Section Clinical Trials

Enhanced Recovery Versus Conventional Care After Cesarean Section

Start date: February 1, 2020
Phase:
Study type: Observational

A protocol of ERACS is introduced to our hospital aiming at saving a lot of time and money for the patients and the population at large .By this way ,free beds for more cases can be available for others patients, so the researcher is welling to study this research on women undergoing CS at Woman's Health University Hospital.

NCT ID: NCT04302597 Completed - Cesarean Section Clinical Trials

Cosmetic Outcomes With Tissue Adhesive (2-octylcyanoacrylate) or Staples in Repeated Cesarean Section

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

Recent clinical trials were developed to test the outcomes of skin closure with tissue adhesive, staples and monofilament synthetic suture after cesarean section with Pfannenstiel incision: both clinical outcomes such as blood loss, surgical site infection, length of postpartum hospitalization, or wound disruption, as well as Patient and Observer Scar Assessment Scale (POSAS) scores 8 weeks after surgery, were comparable between these different skin closure methods. Despite the available studies are often based on robust methodologies and appropriate assessment scales, most of them were aimed to evaluate cosmetic outcomes in primary cesarean section, whereas data analyses published so far do not allow to draw a firm conclusion about repeated cesarean sections. Based on these elements, the aim of this study is to evaluate cosmetic outcomes after skin closure of Pfannenstiel incision with tissue adhesive or staples in a selected population undergoing repeated cesarean section.

NCT ID: NCT04290208 Recruiting - Postoperative Pain Clinical Trials

A Comparison of IV Versus PO Acetaminophen Postoperatively for Opioid Consumption After Cesarean Section

Start date: August 22, 2019
Phase: Phase 4
Study type: Interventional

This randomized controlled study will compare narcotic consumption between two groups: patients that receive a perioperative dose of IV acetaminophen versus patients that receive a perioperative dose of oral liquid acetaminophen for scheduled cesarean section.

NCT ID: NCT04232306 Withdrawn - Postoperative Pain Clinical Trials

Liposomal Bupivacaine + Bupivacaine vs. Bupivacaine Alone on Opioid Use After Elective c/Section

Start date: March 2024
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the effectiveness of local wound infiltration of EXPAREL® (liposomal bupivacaine) with bupivacaine HCl compared to active control with bupivacaine HCl alone following elective primary or repeat cesarean delivery with spinal anesthesia.

NCT ID: NCT04111575 Completed - Cesarean Section Clinical Trials

Music Therapy for Women, Delivered Via Cesarean Section

Start date: February 5, 2018
Phase: N/A
Study type: Interventional

Musical therapy is a type of therapy which is performed under a regular method by adjusting the physiological and psychological effects of musical tones and melodies in accordance with various situations. Therefore, the study was carried out as a randomized controlled trial in order to evaluate the effect of music therapy on the level of pain and anxiety in the postpartum period in women who delivered via cesarean section.

NCT ID: NCT04089176 Completed - Cesarean Section Clinical Trials

Carbetocin Versus Oxytocin for Prevention of Postcesarean Hemorrhage in Pregnancy With High Risk for PPH

Start date: February 1, 2019
Phase: Early Phase 1
Study type: Interventional

Objective: study efficacy of carbtocin versus oxytocin for prevention postpartum hemorrhage in high risk pregnancy who undergo cesarean section

NCT ID: NCT04074005 Recruiting - Cesarean Section Clinical Trials

Incidence and Factors Involving Cesarean Delivery After Epidural Analgesia for Labor

Start date: September 1, 2019
Phase:
Study type: Observational

The rate of cesarean delivery after epidural analgesia for labor has not been reported in our institute. The aim of this study is to elucidate incidence of cesarean delivery in parturient whom received epidural analgesia. Besides, factors associated with the rate of cesarean delivery were studied.