Clinical trials: Pain Monitoring
Anesthesia
Expired Propofol in Low Back Surgery
Edmon (BBraun, Germany) is a portable, commercially available device for measurement of propofol in exhaled air. The study will aim at evaluating the sensitivity and specificity of such exhaled propofol values compared with…
- Trial name
- NCT04771702
- Testing
- Edmon
- Where
- Norway
- Volunteers
- 40 people
- Sponsor
- Oslo University Hospital
Heart Diseases, Atrial Fibrillation (AF)
FAPO-2: Cardiac Patient Monitoring Tool for Clinical Observation and Arrhythmia Detection
The FAPO-2 study (Patient Monitoring Tool for Clinical Observation and Arrhythmia Detection) is a prospective, interventional, non-randomized study designed to evaluate the feasibility, usability, clinical effectiveness, and…
- Conditions
- Heart Diseases, Atrial Fibrillation (AF), Angina, Unstable
- Trial name
- FAPO-2 (NCT07174206)
- Testing
- Smartwatch - all data, Portable holter system, Telemonitoring
- Where
- Brazil
- Volunteers
- 520 people
- Sponsor
- University of Sao Paulo
Pain, Pain, Postoperative
Monitor-Guided Analgesia During General Anesthesia - Part I
This prospective randomized clinical trial evaluates the effects of a monitor-guided opioid analgesia during general anesthesia.
- Conditions
- Pain, Pain, Postoperative, Nociceptive Pain, Opioid Use
- Trial name
- MOGADA (NCT03303651)
- Testing
- Opioid administration in intervention groups, Opioid administration in control group
- Where
- Germany
- Volunteers
- 48 people
- Sponsor
- Universitätsklinikum Hamburg-Eppendorf
Nociceptive Pain, Surgical Procedure, Unspecified
Automatic Remifentanil Administration Guided by ANI During Propofol Anesthesia
Prospective Randomized Monocentric Clinical Trial during propofol anesthesia. The aim of the study is to test whether the use of a medical device designed to automatically administer remifentanil during surgery based on expert…
- Trial name
- ANI-LOOP (NCT03556696)
- Testing
- ANI-REMI-loop, remifentanil pK/pD target administration device, Remifentanil
- Where
- France
- Volunteers
- 52 people
- Sponsor
- University Hospital, Lille
Pain
Safety Study of Analgesia After Craniotomy Surgery With End Tidal (ET) Carbon Dioxide (CO2) Monitoring
This research is being done to compare two methods of giving fentanyl, a narcotic often given to patients following brain surgery and determine if one method has more side effects than the other.
- Trial name
- NCT01327677
- Testing
- Fentanyl
- Where
- United States
- Volunteers
- 137 people
- Sponsor
- Johns Hopkins University
Prostate Cancer, Pain Management
Effect of Rectus Block Timing on Opioid Use
The aim of this study is to observe the effect of administering local anesthetic to the abdominal wall at the beginning or end of surgery under general anesthesia on opioid consumption during surgery.
- Conditions
- Prostate Cancer, Pain Management, Nociception Level Index(NoL), Nociception Monitoring
- Trial name
- PROSTIMERSBOP (NCT07433140)
- Testing
- Early bilateral rectus sheat block, Late bilateral rectus sheat block
- Where
- Turkey (Türkiye)
- Volunteers
- 50 people
- Sponsor
- Koc University Hospital
Pain, Acute, Anesthesia
Pupillary Dilation Reflex Assessment for Intraoperative Analgesic Titration.
In this double blinded randomized controlled study, the pupillary dilation reflex is used for as a nociceptive indicator for opioid administration during elective surgery under general anesthesia.
- Trial name
- PUP-AIT (NCT03248908)
- Testing
- Pupillary dilation reflex, Standard of care
- Where
- Belgium
- Volunteers
- 120 people
- Sponsor
- University Hospital, Antwerp
Pain, Postoperative, Opioid Use
Comparison of Postoperative Nociception Between NOL-guided and Standard Intraoperative Analgesia Based on Fentanyl
Pain is defined as an unpleasant sensory and emotional conscious experience, associated with actual or potential tissue damage. Nociception is the sympathetic response to noxious stimuli during unconsciousness.
- Conditions
- Pain, Postoperative, Opioid Use, Nociceptive Pain, Postoperative Pain
- Trial name
- NOLFentanyl (NCT03858621)
- Testing
- fentanyl NOL guided
- Where
- Chile
- Volunteers
- 100 people
- Sponsor
- Victor Contreras, MSN
Pain
The Efficacy of Pain Management With Self-reporting Pain Monitoring System in Cancer Patient
To compare the pain scales between clinician evaluated and reported with wearable device by patients.
- Trial name
- pain (NCT03117075)
- Testing
- using device for scoring pain scale, named "ANAPA®"
- Where
- 2 sites in South Korea
- Volunteers
- 68 people
- Sponsor
- DERSHENG SUN
Pain
Pain Monitoring Using Plurality of Non-invasive Physiological Measurement
The clinical trial is intended to implement, validate performances and evaluate efficacy of the pain monitoring device for automated assessment of patient's pain level.
- Trial name
- NCT00914173
- Testing
- Scanlaf Circulator and water bath, Medoc TSA 2000
- Where
- Israel
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Medasense Biometrics Ltd
Orthopedic Disorder, Fractures, Bone
Efficacy of Virtual Reality in Pain Reduction in Orthopedic Pediatric Patients
To prospectively determine if pediatric patients undergoing orthopedic procedures can benefit from employing virtual reality for pain management.
- Trial name
- NCT04901793
- Testing
- Virtual Reality Headset and handheld remote control.
- Where
- United States
- Volunteers
- 95 people
- Sponsor
- Ochsner Health System
Respiratory Depression, Postoperative Pain
Incidence of Respiratory Depression in Cesarean Section
This study is designed to determine the incidence and severity of respiratory depression in elective cesarean section patients who have received a spinal or epidural narcotic called duramorph for management of postoperative pain.
- Trial name
- NCT01181843
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Wake Forest University
Monitoring Noxious Events Using EEG-Derived Pain Indices, Procedural Sedation and Analgesia
qNOX Response to Nociceptive Motor Events During Procedural Sedation
The goal of this observational study is to evaluate whether the CONOX monitor can detect pain during sedation in patients undergoing urological procedures.
- Conditions
- Monitoring Noxious Events Using EEG-Derived Pain Indices, Procedural Sedation and Analgesia, Monitored Anesthesia Care
- Trial name
- MO-NOX (NCT07413848)
- Where
- Turkey (Türkiye)
- Volunteers
- 120 people
- Sponsor
- Ankara University
Ovarian Neoplasm
Impact of Specific Monitoring of Intraoperative Analgesia Under General Anesthesia on Chronic Pain After Ovarian Cancer Surgery
This is a single-center, randomized, phase II, non-comparative, single-blind clinical study that will determine whether morphine reduction through intraoperative monitoring by ANI (Analgesia Nociception Index) significantly…
- Trial name
- MONIALC (NCT04906187)
- Testing
- Arm A : intraoperative ANI monitoring of nociception, Arm B : no specific monitoring of nociception
- Where
- France
- Volunteers
- 126 people
- Sponsor
- Institut Bergonié
Prostate Cancer (Adenocarcinoma), Prostate Cancer (Post Prostatectomy)
Robotic Prostatectomy Artificial Intelligence Low Pressure Pain (RALP) Trial
The 'Robotic Prostatectomy Artificial Intelligence Low Pressure Pain Study Trial' aims to assess the feasibility of being able to review operative outcomes such as pain when comparing two commonly used surgical devices for the…
- Conditions
- Prostate Cancer (Adenocarcinoma), Prostate Cancer (Post Prostatectomy), Prostate Cancer Surgery, Prostate Cancers
- Trial name
- NCT06915909
- Testing
- surgery
- Where
- United Kingdom
- Volunteers
- 100 people
- Sponsor
- East and North Hertfordshire NHS Trust
Pain
Assessment of Pain Monitoring With ANI/NIPE Monitor Program in Pediatric Cardiac Surgery Postoperative.
The main objective is to assess correlation between ANI/NIPE values and external evaluation COMFORT B scale during painful medical cares and during said comfort medical cares in intubated children admitted in pediatric intensive…
- Trial name
- ANI/NIPE (NCT02834481)
- Testing
- ANI/NIPE
- Where
- France
- Volunteers
- 20 people
- Sponsor
- University Hospital, Toulouse
Birth, Intrapartum
The Effect of Wireless Electronic Fetal Monitoring on Labor Pain and Birth Experiences
This study is using Electronic Fetal Monitoring (EFM) to assess fetal health in pregnant women in labor. This will be compared with continuous wired EFM and continuous wireless EFM.
- Trial name
- NCT07233187
- Testing
- Continuous Wireless EFM Group
- Where
- Turkey (Türkiye)
- Volunteers
- 112 people, healthy volunteers welcome
- Sponsor
- Tokat Gaziosmanpasa University
Hernioplasty, Cholecystectomy, Laparoscopic
Intensive Monitoring of Post-surgery Pain in Major Ambulatory Surgery
Moderate to severe acute postoperative pain (APP) during part of the postoperative period is a barrier that hinders the central objective of perioperative medicine, which is to achieve an optimal postoperative recovery process.
- Conditions
- Hernioplasty, Cholecystectomy, Laparoscopic, Haemorrhoidal Surgery, Knee Arthroscopy
- Trial name
- NCT07252817
- Testing
- Intensive monioring group, Standard monitoring group
- Where
- Spain
- Volunteers
- 280 people
- Sponsor
- Consorci Sanitari del Maresme
Postoperative Ocular Inflammation, Postoperative Ocular Pain
A Phase 3 Study Evaluating the Safety and Efficacy of TRIESENCE® (Injectable Suspension) for the Treatment of Ocular Inflammation and Pain After Ophthalmic Surgery
This study is designed to evaluate the safety and efficacy of TRIESENCE® (triamcinolone acetonide injectable suspension) in patients undergoing ophthalmic procedures.
- Trial name
- NCT07832552
- Testing
- TRIESENCE (triamcinolone acetonide injectable suspension)
- Where
- United States
- Volunteers
- 250 people
- Sponsor
- Harrow Inc
Pain
To Investigate the Impact of Analgesic Management Guided by qNOX Monitoring on the Comfort and Prognosis of Mechanically Ventilated ICU Patients
Purpose: To explore the effect of analgesic management under the guidance of qNOX monitoring on the comfort level and prognosis of patients with mechanical ventilation in ICU.
- Trial name
- NCT05912855
- Testing
- qNOX
- Volunteers
- 110 people
- Sponsor
- Tianjin Medical University General Hospital