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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06297915
Other study ID # 2022/08-45
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 17, 2022
Est. completion date August 1, 2023

Study information

Verified date March 2024
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aimed to evaluate and compare the efficacy of ketamine and lidocaine infusion in patients with chronic peripheral neuropathic pain. Patients who received intravenous ketamine infusion and the other patient group who received intravenous lidocaine infusion were evaluated in the study. Pain scores and quality of life were assessed with scales before treatment at two weeks, two months, and six months after treatment.


Description:

This study, it was aimed to evaluate and compare the efficacy of intravenous infusion of ketamine and lidocaine, which have been known and used in pain management and which have recently increased interest in the treatment of peripheric neuropathic pain.


Recruitment information / eligibility

Status Completed
Enrollment 102
Est. completion date August 1, 2023
Est. primary completion date May 10, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - 18-65 years of age - Patients with peripheral neuropathic pain (radicular neuropathy, diabetic neuropathy, complex regional pain syndrome type 2, traumatic peripheral nerve injury, trigeminal neuralgia, postherpetic neuralgia) - Patients who was evaluated by DN4 scores with of =4 points Exclusion Criteria: - Patients with central nervous system disease . - Patients with cancer related neuropatic pain. - Patients with central neuropathic pain patterns. - Patients with renal, hepatic, cardiovascular, and psychiatric diseases. - Patients whose treatment could not be completed due to side effects or other reasons. - Patients who had lost their follow-up .

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ketamine
Ketamine infusion was administered at 1 mg/kg (in 1 hour)
Lidocain
Lidocaine infusion was administered at 3 mg/kg (in 1 hour)

Locations

Country Name City State
Turkey Hacettepe University Ankara Cankaya

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

References & Publications (4)

Jendoubi A, Naceur IB, Bouzouita A, Trifa M, Ghedira S, Chebil M, Houissa M. A comparison between intravenous lidocaine and ketamine on acute and chronic pain after open nephrectomy: A prospective, double-blind, randomized, placebo-controlled study. Saudi J Anaesth. 2017 Apr-Jun;11(2):177-184. doi: 10.4103/1658-354X.203027. — View Citation

Niesters M, Martini C, Dahan A. Ketamine for chronic pain: risks and benefits. Br J Clin Pharmacol. 2014 Feb;77(2):357-67. doi: 10.1111/bcp.12094. — View Citation

Shteamer JW, Callaway MA, Patel P, Singh V. How effective is ketamine in the management of chronic neuropathic pain? Pain Manag. 2019 Nov;9(6):517-519. doi: 10.2217/pmt-2019-0032. Epub 2019 Oct 15. No abstract available. — View Citation

van der Wal SE, van den Heuvel SA, Radema SA, van Berkum BF, Vaneker M, Steegers MA, Scheffer GJ, Vissers KC. The in vitro mechanisms and in vivo efficacy of intravenous lidocaine on the neuroinflammatory response in acute and chronic pain. Eur J Pain. 2016 May;20(5):655-74. doi: 10.1002/ejp.794. Epub 2015 Dec 18. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Neuropathic Pain Scale Neuropathic Pain 4 Questions (DN4) Before treatment at two weeks, two months, and six months after treatment.The 7 symptoms items are scored by interviewing the patient.The scores are added and a score of 4 or more outout of ,10 point (severe pain ) is suggestive of neuropathic pain.
Primary Pain Rating Scale Numeric Rating Scale Before treatment at two weeks, two months, and six months after treatment.NRS in which individuals rate their pain on an ten-point numerical scale. Zero:''no pain at all' ten-point ''severe pain''
Secondary Quality of Life Scale Short form-12 (SF-12) Before treatment at two weeks, two months, and six months after treatment.12-question survey PCS and the MCS Scores above 50 indicate a better-than-average health-related quality of life, while scores below 50 suggest below-average health.
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