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Comparison Between Bupivacaine and Bupivacaine With Dexmedetomidine in Caudal Block for Post Operative Pain Control

S

Sindh Institute of Urology and Transplantation

Status and phase

Completed
Phase 4

Conditions

Post Operative Pain

Treatments

Drug: Bupivacaine Hydrochloride 0.25% Injection plus Dexmedetomidine 1 microgram/kg body weight
Drug: Bupivacaine Hydrochloride 0.25% Injection Solution

Study type

Interventional

Funder types

Other

Identifiers

NCT05919173
SIUT-ERC-2021/A-258

Details and patient eligibility

About

The aim of this study is to compare the duration of analgesia, sedation, and intra and postoperative hemodynamics. This drug is recently available in Pakistan. To the best of our knowledge, no published data is available in this respect in Pakistan, so this study would in turn help to fill the gap in knowledge in low-resource settings/emerging economy.

Full description

Postoperative pain is an annoying subjective sensation for both children and their parents. Almost 80% of the patients undergoing surgery experience postoperative pain, and 80% of them reported moderate to severe pain intensity. Management of postoperative pain has become a major concern in pediatrics. Results of many studies in different countries show that postoperative pain in children is inadequate. Lee et al showed that one of the main reasons for inadequate treatment of postoperative pain in children is difficulties with pain assessment and concerns related to the side effects of opioid analgesics.

The regional anesthetic technique significantly decreases postoperative pain and systemic analgesic requirements. Caudal block, usually combined with general anesthetic technique is one of the most popular, reliable, and safe anesthesia techniques for abdominal and lower limb surgeries in children but the main disadvantage of caudal analgesia is the short duration of action after a single injection.

Bupivacaine is a long-acting, reliable local anesthetic agent that is used as a caudal analgesic, but different auxiliary agents need to be co-administered to improve its analgesic efficiency. Various additives used in the past to increase the pain-free period postoperatively and to decrease the analgesic requirement such as midazolam neostigmine, ketamine, clonidine, and dexmedetomidine.

Dexmedetomidine is a potent and highly selective alpha 2 adrenergic agonists that has been described as safe and effective in many anesthetic applications and analgesic techniques. In contrast to other agents, it has sympatholytic, analgesic, and sedative effects, and is randomly free from side effects except for manageable hypotension and bradycardia.

Enrollment

60 patients

Sex

All

Ages

2 months to 7 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • ASA 1 & 2
  • elective per-urethral cystolithotripsy

Exclusion criteria

  • History of developmental delay or mental retardation
  • Known or suspected coagulopathy
  • Known allergy to any of the study drugs
  • Any signs of infection at the site of the proposed caudal block
  • Any caudal anatomical deformity

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Bupivacaine 0.25%
Experimental group
Description:
Bupivacaine 0.25% Dose: 1mL/kg body weight
Treatment:
Drug: Bupivacaine Hydrochloride 0.25% Injection Solution
Bupivacaine+DEX
Experimental group
Description:
Bupivacaine 0.25% plus Dexmedetomidine 1microgram/kg Dose: 1mL/kg
Treatment:
Drug: Bupivacaine Hydrochloride 0.25% Injection plus Dexmedetomidine 1 microgram/kg body weight

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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