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Cesarean Section Complications clinical trials

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NCT ID: NCT05856097 Recruiting - Clinical trials for Cesarean Section Complications

Kinesio Taping With and Without Diaphragmatic Breathing in Women After Cesarean Section

Start date: May 4, 2023
Phase: N/A
Study type: Interventional

Cesarean section is a major abdominal surgery and major challenge of it is to manage the pain and make the patient mobile .In spite of the advantageous effects of kinesio taping and diaphragmatic breathing, limited, data reported to study analgesic effects on pain management and mobility restoration in acute phase of cesarean section.. This study will aim to meet the dares which are associated with cesarean section by reducing the incisional pain associated with improvement in physical mobility as a non-pharmacological treatment.

NCT ID: NCT05840367 Recruiting - Clinical trials for Cesarean Section Complications

Mothers' Experience of Category 1 Cesarean Section

Start date: June 1, 2023
Phase:
Study type: Observational

The aim of this qualitative prospective study is to investigate how mothers experience a category 1 cesarean section in a hospital where the partner is present in the operation room during the entire process (induction of general anestesia, cesarean section, possible resuscitation of newborn). Mothers will be included in the study, if they wish to participate, on day 1 or 2 following the cesarean section and a brief, structured interview will be held concerning her experience of the cesarean section. Clinical baseline data regarding the mother, the cesarean section and the infant will be collected from patients files. Mothers will be contacted again three months after the cesarean section, and a semi-structured interview will be held via telephone. At the end of the interview a screening for posttraumatic stress will be performed, using the PTSD-8 tool. The interviews will be recorded and transscribed verbatim. Content of interviews will be analysed using manifest content analysis. NVivo software will be used for coding interviews.

NCT ID: NCT05834140 Recruiting - Clinical trials for Cesarean Section Complications

Effects of MET on PPDH, Neck Pain and Disability After Cesarean Section

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to determine the effect of Muscle Energy Techniques on post dural puncture headache, neck pain and disability after Cesarean Section. .

NCT ID: NCT05739747 Recruiting - Chronic Pain Clinical Trials

Validation of the Gendolcat Score for the Prognosis of Chronic Postoperative Pain in Cesarean Section

Start date: April 1, 2023
Phase:
Study type: Observational [Patient Registry]

Chronic post-surgical pain is a problem that has historically been underestimated. Over the last few years there has been a search for strategies to both predict and prevent its occurrence in patients undergoing surgery. The Gendolcat index is the only predictive model that uses only objective pre-surgical variables to assess the risk of suffering chronic post-surgical pain. However, it is only validated for the following surgeries: thoracotomy, hysterectomy and open inguinal hernia. Our aim is to test whether the Gendolcat model is also valid for cesarean section.

NCT ID: NCT05458518 Recruiting - Clinical trials for Cesarean Section Complications

Caesarean Wound Dressing Removal Study

Cesarean
Start date: July 1, 2022
Phase: N/A
Study type: Interventional

An open labelled randomised trial on the timing of wound dressing removal for emergency caesarean delivery in labour.

NCT ID: NCT05385276 Recruiting - Clinical trials for Cesarean Section Complications

Transverse Supraumbilical Versus Pfannenstiel Incision For Cesarean Section In Morbidly Obese Women

Start date: May 1, 2021
Phase: N/A
Study type: Interventional

cesarean section is one of the most common operative procedures performed in modern obstetrics, that become increasingly common in both developed and developing countries for a variety of reasons today, thus any useful refinement in the operative technique, however minimal, is likely to yield substantial benefits. In morbidly obese women with a panniculus, the supraumbilical incision is a new technique that showed definite advantages over the Pfannenstiel incision that will avoid burying the wound under a large panniculus and affords excellent abdominal exposure, less blood loss, less post-operative pain, earlier ambulation, and shorter hospital stay. All these advantages were attributed to minimal tissue manipulation.

NCT ID: NCT05380531 Recruiting - Opioid Use Clinical Trials

Personalized Perioperative Analgesia Platform (PPAP) for Cesarean Section

PPAP C-Section
Start date: December 5, 2022
Phase: N/A
Study type: Interventional

The purpose of this collaborative CTSA (Clinical and Translational Science Award) application is to develop an innovative perioperative precision analgesia platform (PPAP) to improve analgesia and reduce serious immediate and long-term adverse outcomes of perioperative opioids in breastfeeding mothers and their infants

NCT ID: NCT05264870 Recruiting - Clinical trials for Cesarean Section Complications

Norepinephrine in Caesarian Section

Start date: June 9, 2022
Phase: Phase 4
Study type: Interventional

Postspinal hypotension is a frequent maternal complication in caesarian delivery under neuraxial anesthesia which is most commonly treated with the administration of phenylephrine infusion. In this trial, postspinal hypotension will be treated with norepinephrine. The main objective is to examine the pharmacodynamic and biochemical effect of norepinephrine both on mother and newborn.

NCT ID: NCT05021315 Recruiting - Clinical trials for Cesarean Section Complications

Vaginal Cleaning Using Povidone Iodine Before CS to Reduce Postoperative Wound Infection

Start date: September 15, 2021
Phase: Phase 3
Study type: Interventional

The aim of work to assess the effectiveness of preoperative vaginal cleansing with povidone iodine on reduction of post caesarean section wound infection Research questions: Does vaginal cleaning using povidone iodine before cesarean section has effect on reduction of postoperative wound infection??

NCT ID: NCT04934995 Recruiting - Clinical trials for Cesarean Section Complications

Arm and Ankle Blood Pressure Cuffs During C-Section

Start date: March 14, 2021
Phase:
Study type: Observational

This is a single center prospective self-control study to validate the effectiveness of left uterine displacement after subarachnoid block (SAB) with simultaneous measurements of blood pressure (BP) on the arm and left ankle during surgery in patients undergoing cesarean delivery (CD) at The Ohio State University Wexner Medical Center