Clinical Trials Logo

Cervical Spine Surgery clinical trials

View clinical trials related to Cervical Spine Surgery.

Filter by:
  • None
  • Page 1

NCT ID: NCT06087380 Completed - Clinical trials for Cervical Spine Surgery

Auricular Acupressure on Improving Pain and Heart Variability in Patients After Cervical Spine Surgery

Start date: February 15, 2022
Phase: N/A
Study type: Interventional

The primary objective of this study is to investigate the effectiveness of auricular acupressure in improving post-cervical spine surgery pain and heart rate variability in patients.

NCT ID: NCT06083298 Recruiting - Clinical trials for Cervical Spine Surgery

Multifidus Cervicis and Inter-Semispinal Plane Blocks in Analgesia After Cervical Spine Surgery

Start date: October 20, 2023
Phase: N/A
Study type: Interventional

Major spine surgery with multilevel instrumentation is followed by a large amount of opioid consumption, significant pain, and difficult mobilization Pain is one of the main factors limiting ambulation, increasing the risk of thromboembolism by immobility, and causing metabolic changes that affect other systems. Therefore, individualized pain management with the use of appropriate analgesic techniques is of paramount importance. Moreover, early intervention in rehabilitation aiming at a better postoperative recovery may reduce the length of hospital stay and return to daily activity. Effective pain management is one of the crucial components in enhanced recovery after surgery (ERAS). Numerous regional anesthetic techniques have been used to provide analgesia following cervical spine surgery, including patient-controlled epidural analgesia, cervical paravertebral block, cervical plexus block, cervical erector spinae plane blocks, and local infiltration analgesia, however, each of these techniques has specific limitations that prevent them from being the analgesic technique of choice for such surgeries. Up to the author's knowledge, there is no study done to compare multifidus cervicis plane block versus inter-semispinal plane block in a randomized controlled clinical trial as preemptive analgesia in patients undergoing cervical spine surgery.

NCT ID: NCT05717361 Recruiting - Pain, Postoperative Clinical Trials

Opioid Sparing Anesthesia in Cervical Spine Surgery

Start date: November 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 lidocaine and ketamine in the same syringe versus remifentanyl analgesia in cervical spine surgery.

NCT ID: NCT04974658 Completed - Clinical trials for Cervical Spine Surgery

Analgesic Efficacy of the Novel Intra- Semispinal Fascial Plane Block in Posterior Cervical Spine Surgery

Start date: August 10, 2021
Phase: N/A
Study type: Interventional

Posterior cervical spine surgery often requires a large posterior midline incision, resulting in poorly controlled postoperative pain, which arises from iatrogenic mechanical damage, intraoperative retraction, and resection to structures such as bone, ligaments, muscles, intervertebral discs, and zygapophysial joints.

NCT ID: NCT04578119 Completed - Clinical trials for Intubation;Difficult

Optimal Intubating Technique Using Videolaryngoscopy in Patients With Semi-rigid Neck Collar

Start date: October 7, 2020
Phase: N/A
Study type: Interventional

In the case of tracheal intubation using a video laryngoscope, both techniques, one is 'conventional technique' in which intubation is performed by placing the blade tip on the vallecula and the other is 'sliding technique' performed by sliding the blade under the epiglottis, are commonly conducted by anesthesiologists. Investigators would like to compare if the sliding technique can improve the condition of tracheal intubation in patients wearing semi-rigid neck collars in cervical spine surgery.

NCT ID: NCT01950702 Recruiting - Clinical trials for Cervical Spine Surgery

Laryngoscope Asssited Lightwand Intubation

Start date: September 2013
Phase: N/A
Study type: Interventional

To evaluate the success rate for intubation of laryngocope assisted lightwand intubation.