Clinical trials: Anesthesia, Recovery
Suprainguinal Fascia Iliaca Block, Varicose Veins
Regional Anesthesia and Recovery After Varicose Vein RFA
This prospective observational study aims to compare the effects of spinal anesthesia and supra-inguinal fascia iliac block (SIFIB) on the quality of postoperative recovery in endovenous radiofrequency ablation (RFA) of varicose…
- Conditions
- Suprainguinal Fascia Iliaca Block, Varicose Veins, Radiofrequency Ablation, Regional Anaesthesia
- Trial name
- NCT07514000
- Testing
- Spinal anesthesia (heavy bupivacaine), SUPRAINGUINAL FACIA ILIACA BLOCK
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people
- Sponsor
- Zonguldak Bulent Ecevit University
Benign Prostatic Hyperplasia
UroLift System TOlerability and ReCovery When Administering Local Anesthesia
The purpose of the study is to evaluate procedure tolerability and surgical recovery following the UroLift® system procedure when conducted with local anesthesia in subjects with symptomatic benign hyperplasia (BPH).
- Trial name
- LOCAL (NCT01876706)
- Testing
- UroLift® System
- Where
- 7 sites in United States
- Volunteers
- 51 people
- Sponsor
- NeoTract, Inc.
Pain, Nausea
Quality of Recovery After Day Care Surgery With App Controlled Remote Monitoring: a Randomized Controlled Trial
Non blinded randomized controlled trial with mixed methods design. To assess the experienced quality of recovery after day care surgery between patients provided with remote home monitoring and patients receiving standard…
- Conditions
- Pain, Nausea, Vomiting
- Trial name
- QuReMo (NCT05244772)
- Testing
- Remote monitoring
- Where
- 3 sites in Netherlands
- Volunteers
- 310 people
- Sponsor
- Onze Lieve Vrouwe Gasthuis
Hemodynamics, Postoperative Recovery
Effect of Ciprofol Infusion for Induction and Maintenance on Hemodynamics and Postoperative Recovery
To study the Effect of Ciprofol Infusion for Induction and Maintenance of anesthesia on Hemodynamics and Postoperative Recovery in Patients Undergoing Thoracoscopic Lobectomy:a randomized, controlled trial.
- Conditions
- Hemodynamics, Postoperative Recovery, Anesthesia
- Trial name
- NCT05664386
- Testing
- propofol, ciprofol
- Where
- China
- Volunteers
- 126 people
- Sponsor
- Xiumei Song
Delayed Emergence From Anesthesia
Effect of Calling the Patient's Name on Recovery From General Anesthesia
The purpose of this study is to find if we can shorten the recovery time by calling the patient's name during anesthesia reversal.
- Trial name
- NCT02149745
- Testing
- Calling the patient's name, Not calling the patient's name
- Where
- South Korea
- Volunteers
- 101 people
- Sponsor
- Seoul National University Hospital
Kyphoplasty, Prone Position
TCI Versus Manual TIVA for Sedation During Prone Kyphoplasty: Effects on Respiration, Recovery, and EEG
This single-center, prospective, observational study compares target-controlled infusion (TCI) versus manually administered total intravenous anesthesia (TIVA) for sedation in patients undergoing kyphoplasty in the prone…
- Conditions
- Kyphoplasty, Prone Position, Target Controlled Infusion of Propofol, End Tidal Carbon Dioxide
- Trial name
- NCT07745348
- Testing
- Target controlled infusion of propofol, non invasive ETCO2 monitoring
- Where
- Turkey (Türkiye)
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Marmara University Pendik Training and Research Hospital
Intraoral Tumor
Differences in Speed of Recovery From Anesthesia for Intraoral Surgery
The goal of this clinical trial is to compare two groups of patients going in general anesthesia for intraoral surgery, the first group TIVA with propofol and the second group inhalational with sevoflurane.
- Trial name
- PSIOS (NCT06275087)
- Testing
- Propofol, Sevoflurane
- Where
- Croatia
- Volunteers
- 50 people
- Sponsor
- Clinical Hospital Centre Zagreb
Recovery
Comparison of Recovery From General Anesthesia in Remimazolam With Flumazenil vs. Propofol
This prospective randomized trial aims to compare recovery time from discontinuation of remimazolam followed by flumazenil administration vs.
- Trial name
- NCT05435911
- Testing
- REMIMAZOLAM BESYLATE 2.5 Mg in 1 mL INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, for SOLUTION [BYFAVO], Flumazenil, Propofol
- Where
- South Korea
- Volunteers
- 66 people
- Sponsor
- Seoul National University Hospital
Cardiovascular Surgery, Regional Anaesthesia
Fascial Plane Blocks In Cardiac Surgery
The aim of the present study is to evaluate the effects of the recto-intercostal fascial plane block (RIFPB) or the rectus sheath block (RSB) combined with the pectoral-intercostal fascial plane block (PIFPB) on postoperative…
- Conditions
- Cardiovascular Surgery, Regional Anaesthesia, Postoperative Analgesia
- Trial name
- NCT07622823
- Testing
- PIFPB + RIFPB, PIFPB + RSB, Control
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Antalya Health Sciences University
Opioid Analgesia, Quality of Recovery (QoR-15)
Effect of Patient Preference for Intraoperative Opioid Use on Early Postoperative Quality of Recovery
Substituting the administration of opioids with a combination of alternative analgesics, known as opioid-free anesthesia (OFA), is gaining in popularity today and is typically administered as part of a larger multimodal strategy.
- Conditions
- Opioid Analgesia, Quality of Recovery (QoR-15), Outcome Assessment, Opioid Free Anesthesia
- Trial name
- PERFECT (NCT06855641)
- Testing
- Opioid based Anesthesia, opioid free anesthesia
- Where
- 2 sites in United States
- Volunteers
- 240 people
- Sponsor
- University of California, Los Angeles
Neurosurgery, Delirium - Postoperative
Electroencephalogram Predicts Post-operative Delirium
The goal of this observational study is to investigate the predictive value of sub-hairline electroencephalography (EEG) during anesthesia recovery for postoperative delirium (POD).
- Conditions
- Neurosurgery, Delirium - Postoperative, Brain Tumor Adult
- Trial name
- EPOD (NCT06894238)
- Testing
- Sub-hairline EEG Monitoring
- Where
- 2 sites in China
- Volunteers
- 137 people
- Sponsor
- Beijing Sanbo Brain Hospital
Hip Surgery, Postoperative Pain Management
Comparison of Intermittent Bolus vs. Continuous Infusion PENG Block for Postoperative Pain in Hip Surgery
This retrospective study evaluates the effects of two different administration methods of the Pericapsular Nerve Group (PENG) Block on postoperative pain control, opioid consumption, and recovery in patients undergoing hip…
- Conditions
- Hip Surgery, Postoperative Pain Management, Pericapsular Nerve Group Block (PENG Block), Regional Anesthesia
- Trial name
- ICPENG (NCT06834243)
- Testing
- Intermittent Bolus PENG Block, Continuous Infusion PENG Block
- Where
- Turkey (Türkiye)
- Volunteers
- 82 people
- Sponsor
- Onur Baran
Hyperthermia, Colorectal Neoplasms
Impact of an Optimised Monitored Anesthesia on the Patients' Recovery After Cytoreduction Surgery Plus HIPEC
The objective of our PILOT study is to evaluate the impact of a controlled (monitored) randomized anesthesia during cytoreductive surgery with HIPEC to oxaliplatin in order to treat adenocarcinomas of colorectal origin.
- Conditions
- Hyperthermia, Colorectal Neoplasms, Oxaliplatin
- Trial name
- CHIPNOL (NCT04104334)
- Testing
- Remifentanil infusion, desflurane titration and fluid infusion will be guided by NOL index, BIS index and Flotrac EV1000 system respectively, Remifentanil infusion and desflurane titration will be guided by anesthesia usual practices
- Where
- Canada
- Volunteers
- 9 people
- Sponsor
- Ciusss de L'Est de l'Île de Montréal
Anesthesia
Administration of Dexmedetomidine Guided by Entropy/SPI Reduce
Dexmedetomidine, a selective alpha2-adrenergic agonist is known to reduce propofol and opioid requirements due to its sedative and analgesic properties.
- Trial name
- NCT02818621
- Testing
- Group Dex (dexmedetomidine)
- Where
- South Korea
- Volunteers
- 64 people
- Sponsor
- Gangnam Severance Hospital
Endoscopic Surgical Procedure
Sedation for Endoscopic Procedures
Endoscopic procedures for biliary strictures, stenting or drainage (ERCP) and ultrasonic imaging or biopsies (EUS) are performed under sedation or anesthesia.
- Trial name
- SEEUPP (NCT05038917)
- Where
- Sweden
- Volunteers
- 500 people
- Sponsor
- Ostergotland County Council, Sweden
Arthroplasty, Replacement, Knee
Testing Regional Anesthesia Techniques for Up and Early Discharge Following Knee Arthroplasty - A Feasibility Study
To assess feasibility of a a trial investigation postoperative patient-reported quality of recovery after total knee arthroplasty (TKA) with periarticular joint injection (PAI) ± single shot adductor canal block with or without…
- Trial name
- TRUE KnORTH 2 (NCT06054750)
- Testing
- Ropivacaine, Normal saline
- Where
- Canada
- Sponsor
- McMaster University
Pain, Postoperative
Biobehavioral Recovery From Surgery and Anesthesia
Reducing postoperative pain leads to increased patient comfort and facilitates speedy recovery and discharge from the hospital following surgery.
- Trial name
- NCT00176696
- Testing
- Use of FACE monitor and BIS monitor
- Volunteers
- 20 people
- Sponsor
- University of Medicine and Dentistry of New Jersey
Anesthesia, Intravenous
Comparison of Recovery Profile After TIVA Between Remimazolam With Flumazenil and Propofol
This prospective, randomized, single-blinded study is designed to compare the recovery profile between propofol-based total intravenous anesthesia (TIVA) and remimazolam-based TIVA in patients undergoing thyroidectomy.
- Trial name
- NCT05047939
- Testing
- remimazolam-based TIVA, propofol-based TIVA
- Where
- South Korea
- Volunteers
- 58 people
- Sponsor
- Seoul National University Hospital
Surgery, Pain
Clinical Evaluation of Medasense Pain Monitor Performances
In this study, the performances of Medasense's non-invasive pain monitoring is compared with standard pain related indicators, such as heart rate, galvanic skin response, etc. , and with a subjective pain level assessment.
- Conditions
- Surgery, Pain, Postoperative Pain
- Trial name
- NCT01631695
- Where
- Israel
- Volunteers
- 96 people
- Sponsor
- Medasense Biometrics Ltd
Quality of Recovery (QoR-15), Quality of Recovery From Anaesthesia
Validation of the Setswana Translated Quality of Recovery Questionnaire in Orthopaedic Patients at a Tertiary Hospital in South Africa
This observational study aims to evaluate the validity, reliability and feasibility of the Setswana-translated version of the 15-item Quality of Recovery (QoR-15) questionnaire.
- Trial name
- NCT07194369
- Where
- South Africa
- Volunteers
- 150 people
- Sponsor
- Sefako Makgatho Health Sciences University