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Cesarean Section Complications clinical trials

View clinical trials related to Cesarean Section Complications.

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NCT ID: NCT04280432 Completed - Clinical trials for Cesarean Section Complications

Monocentric Observational Study: Postoperative Pain After Cesarean Section: Incidence and Risk Factors.

Start date: March 1, 2017
Phase:
Study type: Observational

The purpose of this prospective study was to assess chronic pain 3, and 12 months after cesarean delivery in a cohort of women in University hospital La Paz. We also aim to study the possible contribution of anesthetic and surgical risk factors for the development of Chronic post-surgical pain after cesarean (PCSCP)

NCT ID: NCT04195087 Completed - Clinical trials for Cesarean Section Complications

Perfusion Index and Pleth Variability Index in Cesarean Section.

Start date: December 2, 2019
Phase:
Study type: Observational

The aim of this study is to investigate the predictability of hypotension by using PI and PVI in pre-and post-spinal anesthesia periods in cesarean section cases in the sitting position.

NCT ID: NCT04156282 Completed - Clinical trials for Cesarean Section Complications

Knot Burial Technique for Rectus Sheath Closure

Start date: May 9, 2019
Phase: N/A
Study type: Interventional

Caesarean section is one of the most commonly performed abdominal operations on women in most countries of the world. Its rate has increased markedly in recent years, and is about 20-25% of all child-births in most developed countries. The present study was a step to reduce postoperative pain in cesarean sections. Because of the large number of women that undergo caesarean section, even small differences in post-operative morbidity rates due to different techniques could translate into improved health and significant savings of cost and health services resources. Closing the rectus sheath in cesarean sections with the knots pricking through the skin causes significant postoperative pain, discomfort and delayed ambulation. No comments in literature regarding the best way for closing the rectus sheath in cesarean sections. AIM/ OBJECTIVES The aim of this study is to assess the efficacy of burying knots beneath the rectus sheath during cesarean section in reducing post operative pain and discomfort. Study hypothesis: In women undergoing cesarean sections may or may not burying knots beneath the rectus sheath reduce the post operative pain and discomfort.

NCT ID: NCT04095013 Completed - Clinical trials for Cesarean Section Complications

Intrathecal Bupivacaine-fentanyl and Bupivacaine-dexmedetomidine for Elective Low Segment Caesarean Section

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

the primary objective of the study is to compare the onset and recovery times of sensory and motor blockade of the two study drugs intrathecally with low dose bupivacaine The secondary objectives of the study are to observe hemodynamics, side effects profile, and duration of postoperative analgesia

NCT ID: NCT04086277 Completed - Clinical trials for Cesarean Section Complications

Continuous Intrapartum Support to Reduce Primary Cesarean

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The objective of the study was to evaluate the intervention of intrapartum continuous support by a professional nurse with a university degree to reduce the nulliparous, term, singleton, vertex (NTSV) cesarean birth rate, in women pregnant less than 40 years in the HGZ No. 4 of the Guanajuato delegation of the Mexican Institute of Social Security, Mexico

NCT ID: NCT04070118 Completed - Clinical trials for Cesarean Section Complications

Lower Uterine Segment Thickness and Term Pain,Previous Cesarean Section

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

the purpose of the researchers; The aim of this study is to evaluate the consistency of niche dimensions measured by ultrasonography with visual measurement of the surgeon during the operation of the patient when presenting with pain in her current pregnancy. If patients who have had previous cesarean section present to the emergency department with pain or NST pain, a panic occurs immediately for operation. Purpose of researchers; The aim of this study is to investigate whether a really fine determination of the thickness of the old incision line is associated with full-thickness rupture or incomplete rupture, which appears to be an operation, and if a relationship is found, there is a limit for this thickness.

NCT ID: NCT04069078 Completed - Clinical trials for Cesarean Section Complications

Hyoscine Butylbromide for Prevention of Bradycardia During Cesarean Section

Start date: October 10, 2019
Phase: Phase 4
Study type: Interventional

The aim of this study is to assess the efficacy of Iv hyoscine butylbromide in preventing Bradycardia during cesarean section under spinal anaesthesia with local anaesthetic and morphine.

NCT ID: NCT04046510 Completed - Clinical trials for Cesarean Section Complications

Comparaison of 3 Protocols of Ocytocin Administration in C Section

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

This study aimed to compare 3 doses of ocytocin in bolus injection and contnious perfusion during C section. these doses determined by: high, intermediate and low doses, were administred to parturients during elective or urgent C section under spinal anesthesia

NCT ID: NCT04005664 Completed - Clinical trials for Cesarean Section Complications

Prophylactic Phenylephrine Co-administration During Caesarean Section

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

This single centre prospective alternating intervention study will aim to compare prophylactic phenylephrine given in the first litre of Ringers lactate as co-load in healthy patients having an elective caesarean section under spinal anaesthesia at Edendale Hospital to the existing national protocol guideline - for the treatment of obstetric spinal hypotension.

NCT ID: NCT03968783 Completed - Clinical trials for Cesarean Section Complications

The Effect of Suturing Material on Scar Healing

Start date: May 27, 2019
Phase: N/A
Study type: Interventional

We want to compare the effects of 2 suture materials (monofilament and multifilament) on healing of the uterine scar after a cesarean delivery.