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Post-operative Recovery clinical trials

View clinical trials related to Post-operative Recovery.

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NCT ID: NCT05081232 Withdrawn - Clinical trials for Post Operative Recovery

Continence and Potency Following Multi-Layer Perinatal Issue alloGraft

Start date: January 2024
Phase: N/A
Study type: Interventional

The purpose of this research is to determine the effectiveness of using human Umbilical Cord (UC) allograft to help improve return to erectile function and bladder control in patients following robot-assisted radical prostatectomy (RARP).

NCT ID: NCT04863651 Recruiting - Clinical trials for Cesarean Section Complications

Attachment Predicts Post Cesarean Pain

Start date: January 13, 2020
Phase:
Study type: Observational

The Adult Attachment Style (AAS) is a questionnaire designed to measure how an adult generally feels in their close personal relationships. The questionnaire has two main axes of measurements - avoidance and anxiety, that gives rise to four different categories of attachment styles. Women's attachment styles have been shown to be correlated to pain during labour, but not after. No study has analyzed whether attachment styles are correlated to the pain after cesarean section. This study will assess correlation between the AAS score, and pain after elective cesarean section. Additionally, this study aims to clarify the correlation between attachment scale and overall quality of recovery after cesarean section as defined by a recently validated tool, the ObsQoR10.

NCT ID: NCT03680391 Not yet recruiting - Clinical trials for Post Operative Recovery

Effect of Early Posroperative Feeding on Gastrointestinal Function After Cesarean Section

Start date: September 2018
Phase:
Study type: Observational

Two hundred women were recruited, with 103 randomized to traditional feeding and 97 to early feeding and compare women satisfaction during discharge from hospital

NCT ID: NCT01844960 Completed - Surgery Clinical Trials

Laparoscopic Single Incision -Vs- Multiple Incision Gastric Band Surgery

SIMIS
Start date: November 2011
Phase: N/A
Study type: Interventional

A double blinded randomised control trial comparing the differences between laparoscopic single incision versus multiple port bariatric surgery in morbidly obese patients (BMI>35). Single incision surgery is a new minimally invasive surgical technique requiring the surgeon to operate through one small single incision and is virtually scarless. The traditional laparoscopic approach to abdominal surgery is through multiple small incisions (4-7 ports) across the whole abdomen. This study seeks to identify the risks, benefits and costs of the adjustable gastric band insertion via single incision and multiple incision within the morbidly obese patient group.