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Cesarean Section clinical trials

View clinical trials related to Cesarean Section.

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NCT ID: NCT04457921 Completed - Pain, Postoperative Clinical Trials

Deep Tissue Massage on Pain and Comfort After Cesarean

Start date: May 10, 2019
Phase: N/A
Study type: Interventional

The aim of this study to determine the effect of deep tissue massage applied to the back on pain and comfort after cesarean section. Personal information form was used as data collection form, Visual Analog Scala was used to assess pain, and Postpartum Comfort Questionnaire was used to assess comfort.

NCT ID: NCT04442997 Completed - Cesarean Section Clinical Trials

Use of Cesarean Birth at Private Health Facilities in Lilongwe and Blantyre, Malawi

Start date: February 21, 2022
Phase:
Study type: Observational

The purpose of the research study is to collect preliminary data to which future outcomes after implementing quality improvement projects or research will be compared. There will be observation of the labor and delivery services received and resulting outcomes of women and infants who deliver at private health facilities in urban Malawi. Data will be collected at admission, delivery, and discharge from women and providers on patient characteristics, labor and obstetric characteristics, delivery factors, and pregnancy outcomes that result during the course of the hospitalization. This will include the vital status of the mother and the infant. The overall hypothesis is that cesarean birth rates will be higher than the ecologically supported 10% cesarean birth rate, and that there may be cesareans that are performed without clear medical indication.

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: 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: 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: NCT04050059 Completed - Pain Clinical Trials

Comparison of Two Analgesic Pretreatment Techniques Before Spinal Needle Insertion for Pain Reduction and Maternal Satisfaction Level Assessment in Women Undergoing LSCS.

Start date: November 13, 2019
Phase: N/A
Study type: Interventional

Nowadays lower segment cesarean sections are preferably carried out under regional anesthesia due to multiple advantages. Local infiltration of lidocaine or any other anesthetic is used before lumber puncture in many centers to reduce needle stick pain. EMLA (eutectic mixture of local anesthetic) cream is the combination of lidocaine and prilocaine which have been effectively used in few studies to reduce needle prick pain. We would like to see which analgesic pretreatment is superior in terms of reducing pain of spinal needle insertion and have better maternal satisfaction levels.

NCT ID: NCT04000308 Completed - Analgesia Clinical Trials

QLB vs. Wound Infiltration in Cesarean Section

Start date: August 28, 2019
Phase: N/A
Study type: Interventional

Effective postoperative analgesia after cesarean section (CS) is important because it enables early ambulation and facilitates breast-feeding. A 2009 Cochrane review concluded that wound infiltration with local analgesic after CS reduced opioid consumption. In addition, two regional anesthetic techniques, the transversus abdominis plane (TAP) block and the quadratus lumborum block (QLB), have been shown in multiple studies to reduce post-operative opioid consumption after CS. A recent randomized controlled trial showed that QLB is more effective in reducing morphine consumption post-CS compared to TAP. No randomized controlled trial to date, however, compared the analgesic effect of QLB with infiltration of the wound after CS. The objective of the study is to compare the analgesic effect of QLB type 2 with wound infiltration after CS.