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Lumbar Spine Surgery clinical trials

View clinical trials related to Lumbar Spine Surgery.

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NCT ID: NCT06303557 Recruiting - Clinical trials for Erector Spinae Plane Block

Effect of ESPB on Intraoperative Remifentanil Consumption

Start date: January 31, 2024
Phase: N/A
Study type: Interventional

In recent years, regional anesthesia techniques have also been frequently applied to patients for pain relief. Erector spinae plane block (ESPB), is among the regional anesthesia techniques frequently used in lumbar spine surgery. General anesthesia (GA) is the main method of anesthesia for lumbar spine surgery. However, GA can only inhibit the projection system of the cortical limbic system or hypothalamic cortex. GA cannot completely block the transmission of peripheral noxious stimulus to the central nervous system and cannot effectively inhibit the intraoperative stress response. With the addition of peripheral blocks such as ESPB, lower remifentanil consumption, and more stable hemodynamics are expected by providing preemptive analgesia in patients. As a result of all these; it was aimed to compare the intraoperative remifentanil consumption of patients who underwent preoperative ESPB in patients who will undergo lumbar spine surgery resection under GA with those who underwent postoperative ESPB.

NCT ID: NCT06020508 Recruiting - Clinical trials for Lumbar Spine Surgery

Lumoptik BRIGHTPOINT Reflectometer Device for Lumbar Epidural Placement

Start date: September 12, 2023
Phase:
Study type: Observational

The goal of this clinical trial is to test the BrightPoint Epidural device as the first system to use multispectral reflectometry to find the epidural space in lumbar neuraxial procedures requiring epidural needle. The main questions it aims to answer are: 1. Is the device a qualitatively effective secondary confirmation of Loss of Resistance? 2. Is the device a qualitatively effective training tool for educating trainees in how to perform lumbar epidurals? Participants will undergo a neuraxial procedure in which the attending anesthesiologist will use the BrightPoint epidural device to form an opinion on its effectiveness in confirming epidural space access.

NCT ID: NCT05698914 Recruiting - Clinical trials for Chronic Low-back Pain

Telehealth Mindfulness After Spine Surgery

Start date: February 22, 2023
Phase: N/A
Study type: Interventional

The goal of this pilot clinical trial is to compare two behavioral interventions for patients who are recovering from lumbar spinal surgery for a degenerative spine condition. The study aims to answer the following questions: 1. Is it feasible and acceptable to deliver the interventions and conduct the study procedures in this patient population? 2. Do the interventions benefit patients with regard to pain-related, functional, opioid use, and psychosocial outcomes at 3 and 6 months after surgery, and does one intervention have more benefit than the other? Participants will be asked to do the following: 1. Complete self-report questionnaires online before spine surgery, and around 2 weeks, 3 months, and 6 months after spine surgery. 2. Complete a sensory pain task before spine surgery, and around 2 weeks, 3 months, and 6 months after spine surgery. 3. Around two weeks after surgery, participants will be randomly assigned by chance to one of two behavioral interventions - Mindfulness or Education. Participants will then be asked to attend 8, weekly sessions with a study treatment coach over telehealth (online with camera and microphone).

NCT ID: NCT05680259 Recruiting - Pain Clinical Trials

Assessment of the Effects of Maela Connected Follow-up on Well-being and Pain After Lumbar Spine Surgery

HOSPITEL
Start date: October 6, 2022
Phase: N/A
Study type: Interventional

Digital technologies could reduce the length of hospital stay and improve post-operative recuperation after discharge by offering a remote follow-up. No study has investigated the effects of connected follow-up on lumbar spine inpatients. The purpose of this project is to assess the effects of connected follow-up on pain and quality of life after lumbar spine surgery.

NCT ID: NCT05594407 Recruiting - Pain, Postoperative Clinical Trials

Opioid Sparing Anesthesia in Lumbar Spine Surgery

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

The aim of this double blind randomized study will be to investigate the effect of an opioid-free anesthesia regimen with a mixture of dexmedetomidine-lidocaine-ketamine in the same syringe versus remifentanil analgesia in lumbar spine surgery

NCT ID: NCT04794166 Recruiting - Clinical trials for Lumbar Spine Surgery

Symptom Prevalence and Severity in Lumbar Spine Surgery With and Without Dura Rupture

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

The primary purpose of this study is to assess whether lumbar spine surgery patients with dura rupture differ in symptom prevalence and severity from other lumbar spine surgery patients in the early postoperative phase. This is in order to develop a symptom-specific mobilization algorithm (DURAMOB) that can be used to assess whether patients with dura rupture safe can be mobilized earlier after lumbar back surgery to prevent bed rest complications

NCT ID: NCT04233736 Recruiting - Clinical trials for Erector Spinae Plane Block

Erector Spinae Plane Blocks (ESP) for Postoperative Pain in Lumbo-sacral Spine Surgery

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

The goal of this study is to evaluate the analgesic efficacy of bilateral erector spinae plane (ESP) blocks after lumbar and lumbo-sacral spine surgery by assessing postoperative pain scores and opiate requirements as the primary outcome measures. We are aiming to investigate how ESP blocks, performed under ultrasound guidance at the T12 vertebral level, contribute to postoperative pain control. This will be determined by measuring numerical rating pain scores repeatedly following surgery and opiate consumption until patient discharge from hospital. These primary outcome measures will be compared between a treatment group of participants, who will receive ESP blocks and a control group who will receive a sham block. Our primary hypothesis is that ESP blocks significantly reduce postoperative pain and opiate requirements

NCT ID: NCT03918694 Recruiting - Clinical trials for Lumbar Spine Surgery

Vitamin C Supplement for Lumbar Spine Surgery

Start date: April 24, 2019
Phase: N/A
Study type: Interventional

By doing this study, researchers hope to learn effects of Vit C on lumbar spine surgery outcomes.

NCT ID: NCT02257554 Recruiting - Clinical trials for Lumbar Spine Surgery

Comparing Patients' and Surgeons' Expectations of Lumbar Spine Surgery

Start date: September 2014
Phase:
Study type: Observational

The goals of this study are to assess concordance between the patient-surgeon pair regarding expectations of lumbar spine surgery.