Clinical trials: Recovery Quality
Aortic Valve Stenosis, Iron Deficiency
Iron Infusion in Patients Undergoing Transcatheter Aortic Valve Implantation
The aim of the open-label, randomized controlled superiority IRON TAVI trial is to investigate whether intravenous iron therapy (ferric carboxymaltose) improves Health-Related Quality of Life (HRQOL) in patients with severe…
- Conditions
- Aortic Valve Stenosis, Iron Deficiency, TAVI(Transcatheter Aortic Valve Implantation), Cardiovascular Diseases
- Trial name
- IRON TAVI (NCT07370688)
- Testing
- Intravenous ferric carboxymaltose
- Where
- Netherlands
- Volunteers
- 402 people
- Sponsor
- Erasmus Medical Center
Surgical Intervention, Minor
Validation of a Pediatric Pictorial Version of the QOR-15 Postoperatory Functional Recovery Scale - QoR-15 Pédiatric
Consideration from the patient's point of view is an important step in improving postoperative functional recovery. The questionnaire Quality-of-recovery 15 (QoR-15) is a psychometrically validated questionnaire to measure the…
- Trial name
- NCT04453410
- Testing
- Questionnaire Quality-of-recovery 15 (QoR-15)
- Where
- France
- Volunteers
- 153 people
- Sponsor
- University Hospital, Strasbourg, France
Pulmonary Nodule, Liposomal Bupivacaine
Effect of Intercostal Nerve Block With Liposomal Bupivacaine on Quality of Recovery in VATS Partial Pneumonectomy
Video-assisted thoracoscopic surgery (VATS) is a minimally invasive approach for partial pneumonectomy, but postoperative pain remains a major challenge affecting recovery.
- Trial name
- NCT07512635
- Testing
- Bupivacaine Hydrochloride, Bupivacaine liposome
- Where
- China
- Volunteers
- 96 people
- Sponsor
- Sanming First Hospital
Cataract, Education of Patients
The Effect of Preoperative Education Delivered Using the Pecha Kucha Method on the Quality of Recovery
Objective: The aim of this research is to determine the effect of the Pecha Kucha training method on the quality of patient recovery in patient education.
- Conditions
- Cataract, Education of Patients, Postoperative Recovery
- Trial name
- NCT07383168
- Testing
- Education with Pecha Kucha
- Where
- Turkey (Türkiye)
- Volunteers
- 61 people
- Sponsor
- Ankara Yildirim Beyazıt University
Pancreatic Cancer or Distal CBD Cancer
Comparison Between Volatile Anesthetic-desflurane and Total Intravenous Anesthesia With Propofol and Remifentanil on Early Recovery Quality and Long Term Prognosis of Patients Undergoing Pancreatic Cancer and Common Bile Duct Cancer Surgery
Investigators asses whether there is any difference in short term recovery and long term prognosis according to the anesthetic method in patients who undergoing pancreatic cancer and bile duct cancer and undergoing surgery for…
- Trial name
- NCT03447691
- Testing
- Des (volatile anesthetic-desflurane), TIVA (Total intravenous anesthesia with propofol and remifentanil)
- Where
- South Korea
- Volunteers
- 132 people
- Sponsor
- Yonsei University
Sleep Quality
Examining the Differential Effects of Traditional Float-REST on Sleep and Recovery
The objective of this research study is to assess how the implementation of Float-REST affects sleep quality, sleep structure, nocturnal physiology, subjective wellness, recovery from stressors, and resultant effects on…
- Trial name
- NCT05154032
- Testing
- Traditional Float-REST Therapy
- Where
- United States
- Volunteers
- 18 people, healthy volunteers welcome
- Sponsor
- West Virginia University
Pharmacogenetics, Anesthesia
Perioperative Pharmacogenomic Testing
This is a single centre, prospective feasibility study and pilot randomised controlled trial of patients scheduled for elective intermediate or major non-cardiac surgery.
- Trial name
- PPGx (NCT05063838)
- Testing
- Pharmacogenomic optimisation of anaesthetic medications
- Where
- Australia
- Volunteers
- 200 people
- Sponsor
- Peter MacCallum Cancer Centre, Australia
Hepatectomy, Intertransverse Process Block
Intertransverse Process Block for Quality of Recovery Post-Open Hepatectomy
The study aims to assess the analgesic efficacy of the ITPB at the retro-SCTL space in patients undergoing major open hepatectomy surgery.
- Conditions
- Hepatectomy, Intertransverse Process Block, Quality of Recovery (QoR-15)
- Trial name
- ITPB QoR (NCT06957041)
- Testing
- Intertransverse process block
- Volunteers
- 20 people
- Sponsor
- Chinese University of Hong Kong
Breast Hypertrophy
ESPB Versus Intravenous Lidocaine for Pain After Mastopexy
Elective breast reduction surgery is associated with moderate-to-severe postoperative pain and a risk of developing chronic postsurgical pain.
- Trial name
- NCT07687069
- Testing
- Ultrasound - guided Erector Spine Plane Block (ESPB), Intraoperative intravenous lidocaine infusion
- Where
- Poland
- Volunteers
- 80 people
- Sponsor
- Centre of Postgraduate Medical Education
Cancer of Muscle
Functional Outcomes and HRQoL in Upper-extremity Sarcoma Patients After Limb Salvage
This study aims to assess the functional ability and health-related quality of life (HRQoL) of upper extremity sarcoma patients who have undergone limb salvage surgery.
- Trial name
- NCT02380651
- Testing
- Limb salvage
- Where
- 2 sites in Finland
- Volunteers
- 55 people
- Sponsor
- Helsinki University Central Hospital
Pain, Obesity
Ketamine Effect After Laparoscopic Gastric Reduction: A Randomized, Double-Blinded, Placebo Controlled Study
Laparoscopic surgery for gastric reduction is frequently associated with high levels of postoperative pain. Postoperative pain is very often treated with opioids.
- Conditions
- Pain, Obesity, Hypoxia
- Trial name
- NCT01997515
- Testing
- Ketamine
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- Northwestern University
Inflammation Biomarkers, Quality of Recovery (QoR-15)
Comparison of Inflammatory Factors, Pain Scale, and Postoperative Recovery Quality (QOR - 15) in Patients Undergoing Colorectal Cancer Surgery with Conventional General Anesthesia Techniques Compared to General Anesthesia Combined with Epidural Anesthesia At Prof. Ngoerah Hospital
Surgery can increase IL-6 cytokines, triggering inflammation and metastasis. The combination of general and epidural anesthesia has the potential to suppress IL-6, improve the tumor microenvironment, provide analgesia, and…
- Conditions
- Inflammation Biomarkers, Quality of Recovery (QoR-15), Visual Analog Pain Scale
- Trial name
- NCT06784258
- Testing
- General Anesthesia (control group), General Anesthesia combined with epidural anesthesia
- Where
- Indonesia
- Volunteers
- 44 people
- Sponsor
- Udayana University
Post-Surgical Complication, Economic Problems
The ARRC III Trial of Advanced Recovery Room Care (ARRC).
A postoperative high-acuity model of care (ARRC) has been shown, in a prospective cohort study of approximately 850 patients, to produce a marked improvement in patient and hospital outcomes, and hospital costs, in medium risk…
- Trial name
- ARRCIII (NCT05836285)
- Testing
- ARRC, Usual Care
- Where
- Australia
- Volunteers
- 3,000 people
- Sponsor
- University of Adelaide
Uncontrolled Postoperative Pain
Can Post-operative TAP Block Improve Quality of Recovery After C-sections in Patients on Methadone Maintenance?
This is a prospective randomized double-blind placebo controlled study (0.375% Ropivacaine vs. 0.9% saline) designed to evaluate the effectiveness of transverse abdominis plane (TAP) block in the first 48 hours after c-section in…
- Trial name
- TAP (NCT01644864)
- Testing
- 0.375% ROPIVACAINE
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Thomas Jefferson University
Nerve Block, Nephrectomy, Analgesia
TMQLB Versus TPVB for Acute Pain and Quality of Recovery After Laparoscopic Renal Surgery
This trial is a prospective, randomized, single-center, open-label, parallel-arm, blinded-analysis trial, the objective of which is to evaluate the effect of transmuscular quadratus lumborum block (TMQLB) in the pain relief and…
- Trial name
- NCT03414281
- Testing
- TMQLB group 1, TMQLB group 2, TPVB
- Where
- China
- Volunteers
- 30 people
- Sponsor
- Cui Xulei
Preoperative Anxiety, Orthopedic Surgery
Preoperative Anxiety and One-year Patient-reported Outcomes in Orthopedic Surgery Patients Receiving Enhanced Recovery After Surgery or Conventional Care
This study investigates whether an Enhanced Recovery After Surgery (ERAS) program can help orthopedic surgery patients feel less anxious before their operation and recover better one year after surgery, compared to conventional…
- Conditions
- Preoperative Anxiety, Orthopedic Surgery, Patient Reported Outcome (PRO)
- Trial name
- ERAS-APO (NCT07706244)
- Testing
- Enhanced Recovery After Surgery (ERAS) pathway, Conventional care group
- Where
- Taiwan
- Volunteers
- 220 people
- Sponsor
- Buddhist Tzu Chi General Hospital
Intensive Care Unit Syndrome, Relatives
The Effectiveness of a Post-ICU Recovery Program on Relatives
Relatives of intensive care patients are at risk of developing symptoms of anxiety, depression and post-traumatic stress disorder resulting in impaired health-related quality of life (HRQOL).
- Trial name
- RAPIT-II (NCT03264365)
- Testing
- Intervention
- Where
- Denmark
- Volunteers
- 181 people
- Sponsor
- Holbaek Sygehus
Prostate Cancer, Bladder Cancer
Project HERO: Health Empowerment & Recovery Outcomes
Project HERO is a 12-week study of the efficacy of Body Mind Training (BMT, i.e. Tai Chi and Qigong in this project) for reducing fatigue in male cancer survivors.
- Conditions
- Prostate Cancer, Bladder Cancer, Kidney Cancer, Colon Cancer
- Trial name
- HERO (NCT03345563)
- Testing
- Body Mind Training (BMT), Body Training (BT):, Usual Care (UC)
- Where
- United States
- Volunteers
- 113 people
- Sponsor
- Rutgers, The State University of New Jersey
Quality of Recovery
Effects of Transcutaneous Electrical Nerve Stimulation for Postoperative Quality of Recovery After Shoulder Surgery
Transcutaneous Electrical Nerve Stimulation (TENS) has been reported to reduce postoperative pain scores and opioid consumption after postoperative.
- Trial name
- NCT05833113
- Testing
- Transcutaneous Electrical Nerve Stimulation (TENS)
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Karaman Training and Research Hospital
Opioid-use Disorder, Opioid-related Disorders
An Observational Study of Environmental and SocioEconomic Factors in Opioid Recovery
The RECOVER Study will examine clinical, environmental and socioeconomic factors in recovery from opioid use disorder (OUD) over a 24-month period following exit from a Phase III clinical program for a buprenorphine…
- Trial name
- RECOVER® (NCT03604861)
- Testing
- Not applicable - no defined intervention
- Where
- 35 sites in United States
- Volunteers
- 534 people
- Sponsor
- Indivior Inc.