Clinical Trials Logo

Patient Satisfaction clinical trials

View clinical trials related to Patient Satisfaction.

Filter by:

NCT ID: NCT03349151 Completed - Clinical trials for Postoperative Nausea and Vomiting

Postoperative Results of Early Versus On-demand Maternal Feeding After Cesarean Delivery

Start date: November 19, 2017
Phase: N/A
Study type: Interventional

To compare early versus on demand maternal feeding after cesarean delivery regarding gastrointestinal complaints and patient's satisfaction.

NCT ID: NCT03294109 Completed - Pain, Postoperative Clinical Trials

Evaluation of Abdominal Wall Block With Liposomal Bupivacaine for Post-Operative Analgesia in Donor Nephrectomy

Start date: January 1, 2018
Phase: Phase 4
Study type: Interventional

A blinded randomized control trial in living kidney donors. The study group will receive a liposomal bupivacaine Trans Quadratus Lumborum (TQL) block after the induction of general anesthesia. The following study variables will be collected postoperatively following arrival in the post-anesthesia care unit. Current and maximum intensity pain scores will be documented by nurses in Electronic Health Record (EHR). Total opiate dose consumed every 24 hours will be collected from the EHR and pain diary after discharge. Patient satisfaction will be evaluated using the Revised American Pain Society Patient Outcome Questionnaire (APS-POQ-R) 24 hours' post-procedure. Incidence of nausea will be extracted from nursing notes.

NCT ID: NCT03274336 Completed - Clinical trials for Patient Satisfaction

Influence of Audiovisual Aids in the Preanesthetic Interview

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

1000 patients will be asked to fill out a questionnaire about preanesthetic visit right after the interview. On a daily randomization the Groups will be assigned to: Group A = face-to-face interview; Group B = interview plus brochure, Group C= interview plus movie. Evaluation of patient satisfaction und knowledge transfer will be evaluated with a questionnaire filled out right after the interview with the anesthesist.

NCT ID: NCT03243747 Completed - Clinical trials for Patient Satisfaction

Implementation of a Computer-based Questionnaire for Preoperative Evaluation in Anesthesia Ambulance

Start date: October 4, 2016
Phase:
Study type: Observational

Preanesthetic evaluation is a clinical assessment process with purpose of increased patient safety. One focus is review of patient medical history to reduce perioperative morbidity and mortality as well as optimize the daily process in at anesthesia ambulance. The aim of that study is the development and implementation of a practical computer-based individualized and risk-adapted questionnaire for the daily routine

NCT ID: NCT03226028 Active, not recruiting - Pain Clinical Trials

Perioperative Music Listening on Anxiety, Analgesia Use and Patient Satisfaction

Start date: May 4, 2017
Phase: N/A
Study type: Interventional

The capacity of music to relieve pain has been used in many forms of medicines and has been proven to reduce anxiety, pain and need for analgesia in perioperative setting. However, music listening as an inexpensive and duplicable method has not been studied in the local context. The investigators hereby propose a prospective study to recruit women who undergo surgery to evaluate the effectiveness of music in pain relief and post-operative recovery in KKH; as well as the possibility of implementing music listening in perioperative setting. The patients will be offered to listen to one out of several pre-determined lists of music of different genres before, and after surgery. Data including pain score, Hospital Anxiety and Depression Scale (HADS) score, EuroQol-Five Dimensions questionnaire-using Three Levels (EQ-5D-3L), vital signs, analgesia usage and patient satisfaction will be collected in the perioperative period. The collected data shall also be assessed if they are affected by the presence of music, duration of music listening, and the genre chosen by the patients. The investigators believe that this study could help determine the clinical relevance of music for pain relief in local setting, which potentially could reduce patient pain and anxiety caused by surgery. This in turn could allow music listening to be adopted as a non-invasive pain relief intervention in local healthcare settings and further improve patient outcome with lower cost and greater convenience as well as safety.

NCT ID: NCT03221803 Not yet recruiting - Clinical trials for Patient Satisfaction

Patient Satisfaction and Bone Changes for OT Cap and OT Vertical Attachment

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

The purpose of this study aimed to answer a clinical question whether In a patient with bilateral distal extension area, would the metal framework partial denture with OT vertical attachment versus partial denture with OT CAP attachment result in better patient satisfaction?

NCT ID: NCT03197311 Withdrawn - Post Operative Pain Clinical Trials

A Mobile Application for Post-op Analgesic Consumption

Start date: October 2019
Phase: N/A
Study type: Interventional

Surgical extraction of third molars is one of the most common outpatient procedures performed by oral surgeons. The prescription of postoperative narcotic and NSAID analgesics is the standard of care practice to relieve symptoms of pain, swelling, and trismus after these procedures. The majority of these patients do not return for follow up unless they experience a problem. There is limited data on whether the patients use the narcotics as directed and what is their practice of disposal of the remaining medications that were not consumed. In this research the effectiveness of postop analgesic consumption, analgesic disposal practice, pain control, and patient satisfaction will be compared between patients who are randomized to the intervention group who will use a developed mobile application and a control group who will not use the mobile app.

NCT ID: NCT03173794 Withdrawn - Clinical trials for Patient Satisfaction

CommunityRx for Hunger: A Hospital-Based Intervention

Start date: April 2018
Phase: N/A
Study type: Interventional

The goal of this research program is to reduce health disparities by deploying an information-based intervention to increase caregiver utilization of community-based food supports and satisfaction with care among food insecure caregivers of hospitalized children. We will conduct a randomized controlled trial to evaluate, versus usual care, the effects of the CommunityRx-H intervention on caregiver use of food resources (primary), caregiver patient satisfaction with care (primary), caregiver mental health-related quality of life (secondary), and caregiver household food security (secondary). The proposed research will yield an understanding of how to leverage a child's hospitalization to effectively intervene on the problem of food insecurity. Findings will inform the rapidly growing field of healthcare-based interventions to address health-related social needs.

NCT ID: NCT03127033 Not yet recruiting - Clinical trials for Patient Satisfaction

Comparison Between Acrylic and Soft Liner Telescopic Overdentures Regarding Patient Satisfaction

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

Conventional complete overdenture will be made to ectodermal dysplasia patients, a week after delivery and after 3 months Patient satisfaction, retention and periodontal condition will be assessed. the denture will be taken from the patient for 2 weeks.Acrylic telescopes will be replaced with soft liner and again Patient satisfaction, retention and periodontal condition will be assessed a week after delivery and 3 months later.

NCT ID: NCT03026400 Completed - Clinical trials for Patient Satisfaction

Sub vs Trans-umbilical Incision: A Patient's Satisfaction-centered Trial

Start date: August 2014
Phase: N/A
Study type: Interventional

While some studies have suggested that subumbilical and transumbilical incisions have a similar clinical efficiency and safety, no study has yet evaluated their respective impact on patient's postoperative aesthetic satisfaction. The objective of this randomised trial is to compare patient's postoperative aesthetic satisfaction depending on the type of incision which is performed during surgeries.