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Cesarean Section Complications clinical trials

View clinical trials related to Cesarean Section Complications.

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NCT ID: NCT04302545 Completed - Clinical trials for Cesarean Section Complications

Cystoinflation to Prevent Bladder Injury in Multiple Caesarean Sections

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The healthy pregnant women with previous operative deliveries admitted for elective C-section will be counselled and conditioned informed consent will be taken to be included in either study group if dense pelvic adhesions will be found during their operation. Adhesiolysis will be performed using bladder retro-fill with 300cc saline in the cystoinflation group, and without retro-fill in control.Both groups will be observed for bladder injury rate,bloodloss,operativetime,urinary tract infection,micturition problems and fistula formation.

NCT ID: NCT04287933 Not yet recruiting - Clinical trials for Cesarean Section Complications

Role of Drain in Decreasing Postoperative Complications

Start date: March 2, 2020
Phase: N/A
Study type: Interventional

postoperative complications are common after cesarean section

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: NCT04256642 Recruiting - Clinical trials for Cesarean Section Complications

Comparison of the Erector Spinae Plane Block Versus Intrathecal Morphine on Post-Cesarean Delivery Analgesia

ESPCS
Start date: February 2020
Phase: Phase 3
Study type: Interventional

This study is a Randomized Control Trial comparing the Erector Spinae Plane Block with intrathecal morphine for post cesarean delivery analgesia.

NCT ID: NCT04230525 Recruiting - Clinical trials for Cesarean Section Complications

Body Impedance Method in Patients Undergoing Urgent and Elective Cesarian Section

Start date: March 5, 2020
Phase:
Study type: Observational

Independent form anesthetic methods, during C/S, considering both maternal and fetal conditions, some crucial hemodynamic changes can appear and can be claimed non invasively with the whole body bioimpedance. In this research, any kind of hemodynamic difference between this method and urgent or elective C/S case will be detected and the clinic pursuit can be developed creating an advantage in favor of both maternal and fetal conditions.

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: NCT04177966 Recruiting - Anxiety Clinical Trials

The Effect of Pre-operative Videotape Before a Planned Cesarean Section on Anxiety Level

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

The study aim is to examine the relationship between providing information to women prior to elective cesarean delivery and anxiety levels around surgery. the patients will be assigned into two groups - intervention and control. In the intervention group - the day before surgery the women will watch a pre-prepared video showing in detail the course of events around the operation. the level of anxiety, pain level and Intake of Analgesics will be compared between the two groups

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: NCT04125498 Suspended - Clinical trials for Cesarean Section Complications

The S-CARE Trial: Manual Treatment for C-sections Scars, a Pilot Study.

S-CARE
Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study aims to examine the effects of an osteopathic treatment on adhesions related to c-sections scars.

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