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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06438952
Other study ID # E.142568
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 2024
Est. completion date December 2024

Study information

Verified date May 2024
Source Bezmialem Vakif University
Contact Zübeyde Özdemir
Phone +90 2125232288
Email etikkurul@bezmialem.edu.tr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Low back pain is a symptom that is frequently seen in the general population and reduces the quality of life of patients. Conventional medical treatment for patients with low back pain includes oral medication, lifestyle modification, education, exercises, lumbar traction and manual manipulation, heat application, and other interventional procedures. Epidural injections, one of the interventional procedures, are one of the common treatment methods for low back pain, especially caused by disc prolapse. Steroids are commonly used to reduce inflammation in the epidural space. Epidural steroid injection can be given to the lumbar epidural space via transforaminal, interlaminar and caudal routes, and the effectiveness rate of each is different. These interventional methods used to treat low back pain can be applied in combination. The main purpose of this study is to observe how adding lumbar sympathetic blockade will affect the patient's pain in the postoperative period in patients to whom we applied caudal epidural and transforaminal steroid injection.


Description:

Low back pain is a symptom that is frequently seen in the general population and reduces the quality of life of patients. Conventional medical treatment for patients with low back pain includes oral medication, lifestyle modification, education, exercises, lumbar traction and manual manipulation, heat application, and other interventional procedures [1, 2]. Epidural injections, one of the interventional procedures, are one of the common treatment methods for low back pain, especially caused by disc prolapse. Steroids are widely used to reduce inflammation in the epidural space [3, 4]. Epidural steroid injection can be administered to the lumbar epidural space via transforaminal, interlaminar and caudal routes, and each has different efficacy rates [5-7]. Sympathetically maintained pain, including lumbar sympathetic ganglion block (LSGB), complex regional pain syndrome (CRPS) types I and II, neuropathies (such as postherpetic neuralgia, stump or phantom limb pain), diabetic polyneuropathy, and ischemic pain from vascular insufficiency in the lower leg It is a widely applied procedure for diagnosing and managing diseases [8]. The autonomic nervous system consists of sympathetic and parasympathetic departments. As the name suggests, blood supply to the lower extremity increases after lumbar sympathetic block. This is useful in sympathetic system-mediated treatment of pain [9]. The most important reason for adding fentanyl and magnesium as adjvams is to improve the quality of analgesia and provide analgesia for a longer period of time. Both fentanyl and magnesium have the ability to modulate neurotransmitter release and affect neuronal excitability. Fentanyl demonstrates the role of the sympathetic nervous system in modulating pain by increasing the effectiveness of endogenous opioids in the sympathetic ganglia and central nervous system. Magnesium competes with calcium; It reduces the release of neurotransmitters such as acetylcholine. Magnesium's ability to inhibit the release of acetylcholine contributes to its anticonvulsant properties. Additionally, blocking NMDA receptors contributes to its analgesic effects. Additionally, magnesium's ability to enhance the effects of local anesthetics has been studied. By increasing the firing threshold in nerves and causing hyperpolarization, magnesium enhances the effect of local anesthetics, thereby improving nerve blockade. This enhancement of nerve blockade is particularly evident when magnesium is added to agents such as bupivacaine [10, 11]. These interventional methods used to treat low back pain can be applied in combination. There is not enough research on this subject.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 2024
Est. primary completion date November 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - ASA I-II-III - Patients who underwent facet joint injection and transforaminal injection due to lumbar disc herniation Exclusion Criteria: - Patients with known allergies to the drugs to be used in treatment - Infection near the puncture site - Known coagulation disorders - Patients with internal fixation or severe anatomical variation such as scoliosis and tumor - History of sympathetic chemical or thermal neurolysis - Alcohol and drug use - Disorder of consciousness - Liver failure, renal failure, advanced cardiac failure - Uncontrolled diabetes mellitus - Morbid obesity (body mass index (BMI) > 35 kg m-2) - Female patients during pregnancy and breastfeeding - Not approving the informed consent form

Study Design


Intervention

Procedure:
Transforaminal steroid injection combined with lumbar sympathetic blockade
Transforaminal steroid injection will be made with 2 mg dexamethason + 20 mg lidocaine + 5mg bupivacaine + 5 mcg fentanyl + 100mg magnesium under US-guidance Lumbar sympathetic blockade will be made with 5 ml 0.5% bupivacaine + 6 mg dexamethason + 10 ml NaCl
Transforaminal steroid injection only
Transforaminal steroid injection will be made with 2 mg dexamethason + 20 mg lidocaine + 5mg bupivacaine + 5 mcg fentanyl + 100mg magnesium under US-guidance

Locations

Country Name City State
Turkey Aylin Ceren Istanbul
Turkey Aylin Ceren Sanli Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Bezmialem Vakif University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity score Postoperative pain assessed with numeric rating scale (NRS 0: no pain 10:pain as bad as can be ) Preoperative and postoperative 24th hour, 1st week, 1st month and 6th month
Secondary Oswestry Disability Index (ODI) Preoperative and postoperative 24th hour, 1st week, 1st month and 6th month
Secondary Neuropathic pain questionnaire Preoperative and postoperative 24th hour, 1st week, 1st month and 6th month
Secondary Patient satisfaction The patient is asked to give a score between 1 and 10 in terms of satisfaction with the procedure (1 = I am not satisfied with the procedure, 10 = I am very satisfied with the procedure). Patient satisfaction measured using a numeric rating scale 0 to 10 (0 = unsatisfied; 10 =very satisfied)
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