Clinical trials: Recovery
Remazolam Anesthesia, Postoperative Recovery
Effect of Remazolam on Anesthesia Recovery in Patients Undergoing Fundus Surgery
to investigate the effect of remazolam benzenesulfonate in patients with ocular fundus surgery, so as to guide clinical anesthesiologists to choose more appropriate anesthetic drugs in fundus surgery
- Trial name
- NCT06205719
- Testing
- ciprofol, Remazolam, Flumazenil
- Volunteers
- 93 people
- Sponsor
- Sichuan Provincial People's Hospital
COVID-19
Study to Assess the Effect of ONS Nutridrink® 200 ml on the Recovery of Patients With COVID-19 and Respiratory Support
The goal of this low-interventional study was to learn about the effect a nutritional supplement in patients with COVID-19 and respiratory support.
- Trial name
- NCT05579028
- Testing
- Nutridrink ONS 200 ml
- Where
- 6 sites in Russia
- Volunteers
- 185 people
- Sponsor
- Enrollme.ru, LLC
Recovery Methods, Exercise Training
Effects of Different Recovery Methods on Lactic Acid Removal, Flexibility, Strength, and Endurance
The aim of this study is to compare these three different recovery methods following a single bout high-intensity interval exercise program with each other in terms of blood lactate clearance, muscle flexibility, muscle strength…
- Trial name
- NCT03563430
- Testing
- Active Recovery Group, Self-Massage with Foam Roller Group, Neuromuscular Electrical Stimulation
- Where
- Turkey (Türkiye)
- Volunteers
- 45 people, healthy volunteers welcome
- Sponsor
- Biruni University
Lung Cancer, Thoracic Cancer
Exploring Robotic-assisted Thoracic Surgery for Lung Cancer
Background Surgery for lung cancer can be performed using open (thoracotomy) or minimally invasive techniques (Video Assisted Thoracic Surgery (VATS)).
- Conditions
- Lung Cancer, Thoracic Cancer, Surgery
- Trial name
- ROSE (NCT03658083)
- Testing
- Thoracotomy, Robotic-assisted thoracic surgery
- Where
- 2 sites in United Kingdom
- Volunteers
- 55 people
- Sponsor
- Teesside University
Esophageal Cancer
Drainless Robot-assisted Minimally Invasive Esophagectomy
The aim of this study is the evaluation of two different chest drain management strategies in patients undergoing robot-assisted minimally invasive esophagectomy (RAMIE) for esophageal cancer with regard to perioperative…
- Trial name
- RESPECT (NCT05553795)
- Testing
- Early removal of chest drain, Chest drain
- Where
- Germany
- Volunteers
- 49 people
- Sponsor
- Technische Universität Dresden
Major Liver Resection
Trial Using Octreotide to Enhance Liver Recovery After Hepatectomy
This will be a prospective, randomized, double blind trial enrolling patients who will undergo major liver resection. Patients will be randomized in a 1:1 ratio to receive either octreotide or placebo in the postoperative period.
- Trial name
- NCT03179995
- Testing
- Octreotide
- Where
- 2 sites in United States
- Volunteers
- 23 people
- Sponsor
- Fox Chase Cancer Center
Knee Osteoarthritis
Effects of Tele-prehabilitation in Patients Waiting for Knee Replacement
After knee arthroplasty rehabilitation is fundamental to patient's functional recovery, but in recent years there has been a growing interest in the possibility to prepare patients for surgery through a "prehabilitation" program.
- Trial name
- NCT05668312
- Testing
- Tele-prehabilitation, Standard prehabilitation
- Where
- 2 sites in Italy
- Volunteers
- 68 people
- Sponsor
- I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
Colorectal Cancer
Pemetrexed Alone as Salvage Treatment in Metastatic Colorectal Cancer Patients Who Were Failed After Standard Chemotherapy: A Phase II Single Arm Prospective Study
Pemetrexed is an anticancer agent that exerts its action by disrupting crucial folate-dependent metabolic processes essential for cell replication.
- Trial name
- NCT02588781
- Testing
- Pemetrexed
- Where
- South Korea
- Volunteers
- 23 people
- Sponsor
- Samsung Medical Center
Aphasia, Stroke
Effectiveness of Intensive Aphasia Therapy Under Routine Clinical Conditions
The purpose of this study is to examine whether 3 weeks of intensive language therapy provided in clinical in- and outpatient settings is effective in improving everyday communication in postacute/chronic post-stroke aphasia, as…
- Trial name
- FCET2EC (NCT01540383)
- Testing
- Intensive integrative aphasia therapy, Waiting list control group
- Where
- Germany
- Volunteers
- 156 people
- Sponsor
- University Hospital Muenster
Analgesia, Pain Management
Ultrasound-Guided Recto-Intercostal Fascial Plane Block in Laparoscopic Cholecystectomy
The aim of the study is to reduce postoperative pain by performing rectointercostal block in L/S cholecystectomy surgeries. Main goal is to provide well managed post-operative analgesia.
- Conditions
- Analgesia, Pain Management, Pain, Acute Post-Operative
- Trial name
- NCT07745972
- Testing
- Rectointercostal facial plane block using bupivacaine 0.25%
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people
- Sponsor
- Istinye University
Malaria
Trajectories and Mechanisms of Recovery From Malaria: An Observational Study
This observational research study aims to answer the question: 'Which aspects of human biology play an important role in recovery from symptomatic malaria?' In particular, the researchers aim to identify human genes for which the…
- Trial name
- SCRIPT (NCT05149157)
- Testing
- Symptomatic malaria
- Where
- United Kingdom
- Volunteers
- 240 people
- Sponsor
- Imperial College London
Regional Anesthesia Morbidity
Efficacy of SAP Block Versus ESP Block in VATS Surgery
During VATS (Video assisted thoracic surgery) small incisions are made in the patient's chest through which a camera and instruments are inserted to allow a lung operation to be performed.
- Trial name
- ESPvSAP (NCT03862612)
- Testing
- regional anaesthesia with Levobupivicaine 0.25% 30mls with two methods either erector spinae plane block or serratus anterior plane block
- Where
- Ireland
- Volunteers
- 60 people
- Sponsor
- Mater Misericordiae University Hospital
Spinal Surgery
Comparison Between Return and Wastage of Your Own Blood, Collected During Spinal Surgery, for Verification of Safety When Returning Blood
The study is an open, randomized, controlled, single-centre study including a total of 42 evaluable subjects scheduled for spinal surgery with an approximate expected bleeding of 800-1500 ml.
- Trial name
- NCT01251042
- Testing
- Sangvia
- Where
- Denmark
- Volunteers
- 51 people
- Sponsor
- Wellspect HealthCare
Anesthesia, Anesthesia Recovery Period
Effect of Epidural Anesthesia and Analgesia on Quality of Recovery After Radical Prostatectomy.
Postoperative quality of recovery (QoR) could be related to anesthesia and postoperative analgesia. This study is exploring early QoR after radical prostatectomy in the two groups of anesthesia.
- Conditions
- Anesthesia, Anesthesia Recovery Period, Radical Prostatectomy, Patient Satisfaction
- Trial name
- QoR (NCT04587505)
- Testing
- Epidural anesthesia with light general anesthesia, Postoperative epidural analgesia, General anesthesia
- Where
- Croatia
- Volunteers
- 61 people
- Sponsor
- University Hospital of Split
Bladder Cancer
Fast Track Protocol After Radical Cystectomy and Urinary Diversion: A Randomised Controlled Trial.
We will design a randomized controlled single center study in which we will compare 2 groups of patients, 1 with standard perioperative protocols and another one in which we will apply fast track protocols in patients after…
- Trial name
- NCT04939194
- Testing
- Fast Track Protocol
- Where
- Egypt
- Volunteers
- 200 people
- Sponsor
- Mansoura University
Prostate Cancer, Recurrence
Charité HT-Prostate
The combination of regional hyperthermia and salvage radiotherapy is being tested in patients with biochemically recurrent prostate cancer after radical prostatectomy.
- Trial name
- NCT04159051
- Testing
- Regional Hyperthermia
- Where
- 3 sites in Germany
- Volunteers
- 100 people
- Sponsor
- Charite University, Berlin, Germany
Behavior, Health
Peer-Delivered Episodic Future Thinking for Returning Citizens
The goal of this study is to examine the effectiveness of a brief, episodic future thinking (EFT) intervention in a substance use treatment setting serving returning citizens with substance use disorders (SUD).
- Trial name
- NCT06119503
- Testing
- Elongating Time HOrizons for Reentry (ETHoR), Standardized Episodic Thinking (SET)
- Where
- United States
- Volunteers
- 40 people, healthy volunteers welcome
- Sponsor
- Henry Ford Health System
Heart Failure
Interleukin-1 Receptor Antagonist for the Treatment of Heart Failure in Patients With Left Ventricular Assist Devices
Heart failure remains a major cause of morbidity and mortality. Many patients with heart failure receive support from a left ventricular assist device (LVAD) at some point in the course of their disease.
- Trial name
- NCT02547766
- Testing
- Anakinra
- Where
- United States
- Volunteers
- 10 people
- Sponsor
- University of Utah
Traumatic Spinal Cord Injuries
Recovery of Upper Limb Function in Persons With Spinal Cord Injury: Lead-In Study
Many individuals with cervical spinal cord injury (SCI) have difficulty using their hands and arms. MyndMove is a non-invasive medical device that uses short, low energy electrical pulses with surface electrodes to cause muscle…
- Trial name
- MyndMove (NCT02799966)
- Testing
- Myndmove
- Where
- 3 sites in Canada
- Volunteers
- 9 people
- Sponsor
- University of British Columbia
Chronic Ischemic Stroke
CC-101 (f/k/a NR1) Neural Stem Cell Transplantation for Adults With Chronic Ischemic Stroke
The suNR1se II Study is a Phase 2b randomized, controlled, multi-center clinical trial evaluating the efficacy and safety of stereotactic intracerebral administration of CC-101 (f/k/a NR1), an investigational allogeneic neural…
- Trial name
- suNR1se II (NCT07709845)
- Testing
- CC-101 (f/k/a NR1) Intracerebral Transplantation, Tacrolimus
- Volunteers
- 36 people
- Sponsor
- Clarion Cells, Inc.