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Adding Ketamine to Levobupivacaine in Paravertebral Block in Thoracotomy

T

Tanta University

Status and phase

Completed
Phase 4

Conditions

Levobupivacaine
Chronic Pain
Ketamine
Acute Pain
Paravertebral Block

Treatments

Drug: Ketamine + Levobupivacaine
Drug: Levobupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT06011746
36264PR244/6/23

Details and patient eligibility

About

To evaluate the role of adding ketamine to levobupivacaine in PVB on acute and chronic pain in thoracotomy

Full description

Several adjuvants have been added to them to enhance the effects of those blocks. Dexamethasone, morphine, dexmedetomidine, clonidine, ketamine, and magnesium sulphate are some of them. results are variable.

Ketamine blocks N-Methyl-D-Aspartate (NMDA) receptors in the spinal cord. It is also considered to influence voltage sensitive Calcium ions channels, opioid receptors, and monoaminergic receptors. Therefore, it is considered overall to affect nociception.

Enrollment

60 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-75 years.
  • Both sexes.
  • ASA (American Society of Anesthesiology) physical status II-III.
  • Scheduled for open thoracotomy.

Exclusion criteria

  • Contraindications to or failed paravertebral block .
  • Body mass index (BMI) >35 kg/m2.
  • The likelihood of postoperative mechanical ventilation.
  • Patients with coagulopathy, poorly controlled diabetes mellitus, depression or other psychiatric disorders that required antidepressant drugs, alcohol, or recreational drug addiction.
  • Hypersensitivity to ketamine or levobupivacaine.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Ketamine Group
Experimental group
Description:
patients will receive paravertebral block (19 mL of 0.5% levobupivacaine + 1 ml ketamine (50 mg)).
Treatment:
Drug: Ketamine + Levobupivacaine
Control Group
Active Comparator group
Description:
patients will receive paravertebral block (19 mL of 0.5% levobupivacaine + 1 ml normal saline)
Treatment:
Drug: Levobupivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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