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Analgesia, Patient-Controlled clinical trials

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NCT ID: NCT06316921 Completed - Pain, Postoperative Clinical Trials

Epidural PCA on Pain Relief After L-spine Surgery

Start date: June 1, 2021
Phase:
Study type: Observational

This study aimed to evaluate the effect of epidural patient-controlled analgesia (PCA) on postoperative pain relief after lumbar spine surgeries. The eligible patients received two types of postoperative pain management: PCA and standard pain treatment. Comparisons between the two groups were made in terms of postoperative pain level.

NCT ID: NCT05691101 Recruiting - Clinical trials for Brachial Plexus Block

Comparison of Using CIBPB With or Without IV-PCA After Arthroscopic Rotator Cuff Repair

Start date: January 31, 2023
Phase: N/A
Study type: Interventional

The goal of this study is to compare the continuous brachial plexus block with or without intravenous patient controlled analgesia(PCA) in patients undergoing arthroscopic rotator cuff repair, in terms of quality of recovery, postoperative pain score, and adverse event.

NCT ID: NCT05672225 Recruiting - Dexmedetomidine Clinical Trials

Two-channel IV-PCA With Dexmedetomidine

Start date: February 7, 2023
Phase: N/A
Study type: Interventional

Dexmedetomidine was administered in the 'selector' channel and fentanyl in the 'basic & bolus' channel of dual channel intravenous patient-controlled analgesia (IV-PCA) and the amount of opioid consumption was compared. In addition, intensity of pain, postoperative nausea/vomiting, and postoperative delirium was evaluated.

NCT ID: NCT05299866 Recruiting - Cesarean Section Clinical Trials

The Effect of S-ketamine Combined With Sufentanil for Postoperative Analgesia in Patients Following Cesarean Section

Start date: April 12, 2022
Phase: Phase 4
Study type: Interventional

This randomized controlled trial is designed to investigate the effect of low-dose of S-ketamine combined with sufentanil for postoperative patient-controlled intravenous analgesia in patients following cesarean section.

NCT ID: NCT05188794 Completed - Clinical trials for Postoperative Pain, Acute

Comparison of Two Different Approach TAP Block on Pain Management of Laparoscopic Nephrectomy

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Primary aim is to compare the effectiveness of the posterior approach Transversus abdominis plane block (P-TAP) and the lateral approach Transversus abdominis plane block (L-TAP) technique on the pain management of the laparoscopic nephrectomy in terms of visual analog pain scale and postoperative opioid consumption. Secondary aim is to compare complication rates of the two techniques.

NCT ID: NCT04111328 Completed - Clinical trials for Analgesia, Patient-Controlled

the Effect of Different Drugs and Infusion Ways on Degree of Postoperative Comfort

Start date: October 8, 2019
Phase: Phase 4
Study type: Interventional

To explore the effect of different drugs and infusion ways on degree of postoperative comfort.Patients undergoing spinal neoplasm surgery receive different patient controlled analgesia(PCA) drugs postoperatively,one group is sufentanil,the other is hydromorphone. Then each drug group will be divided into two subgroups according to the infusion way,intravenously,subcutaneously. During the patient controlled analgesia period, patients' degree of comfort,pain score,sleep quality, the degree of side reaction will be recorded.

NCT ID: NCT03919916 Recruiting - Pain Clinical Trials

Serratus Plane Block With Parenteral Opioid Analgesia Versus Patient Controlled Analgesia in Rib Fractures

COPE
Start date: May 28, 2021
Phase: N/A
Study type: Interventional

In this multicentre randomised controlled trial, adult patients with isolated chest trauma and two or more unilateral rib fractures will be randomised to either serratus plane block and patient controlled analgesia or patient controlled analgesia alone. Our primary outcome is the static visual analogue scale score at one hour.

NCT ID: NCT03846102 Terminated - Pain Clinical Trials

MORphine Use in the Fascia Iliaca Compartment Block With UltraSound

MORFICUS
Start date: January 28, 2019
Phase: Phase 4
Study type: Interventional

Appropriate management of analgesia for proximal femoral fractures is a common problem in the emergency department (ED). Side effects from morphine usage such as nausea, vomiting, respiratory depression, sedation, and obstipation are especially pronounced in elderly. Fascia Iliaca Compartment Block (FICB) holds promise as a simple and safe, and effective alternative method to reduce pain. Local anaesthetic injected in the anatomic space underlying the fascia iliaca, spreads to block the nerves traversing it. This regional anaesthesia includes the femoral nerve. Previous studies in the ED showed promise but lacked blinding, involved low numbers of subjects, or did not use ultrasound localisation of the injection site. The latter is becoming common practice. In this randomised placebo controlled trial the FICB with ultrasound localisation of injection of levobupivacaïne will be compared to the FICB with placebo. It aims to prove that less morphine is used in the intervention group. Other research parameters are pain scores and minor adverse events related to morphine use.

NCT ID: NCT03813225 Recruiting - Pain, Postoperative Clinical Trials

Bilateral Serratus Intercostal Plane Block for Myocardial Revascularization (SERRINT)

SERRINT
Start date: January 15, 2019
Phase: N/A
Study type: Interventional

Two-parallel arm, double-blind, individually randomized controlled trial. Primary endpoint: Fentanyl consumption in the first 48 postoperative hours. Secondary endpoints: Pain at rest, Pain on movement, stay in ICU, Postoperative nausea and vomiting (PONV), sedation, Hemothorax, seizures, arrythmias

NCT ID: NCT03685188 Enrolling by invitation - Clinical trials for Analgesia, Patient-Controlled

Oxycodone and Sufentanil for Analgesia in Hip Surgery

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

We design this randomized controlled trial to compare the safety and efficacy of Oxycodone and Sufentanil for postoperative patient-controlled analgesia in patients undergoing hip surgery, with a view to finding the optimal postoperative analgesic regime with fewer adverse reactions and promoting patients' rehabilitation.