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Clinical Trials/CTRI/2024/03/063604
CTRI/2024/03/063604
Not yet recruiting
Phase 3

ltrasound-guided quadratus lumborum block versus ultrasound-guided caudal epidural block for post-operative analgesia in children undergoing lower abdominal surgeries: A prospective randomized controlled study - NI

All india institute of medical sciences Raipur0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: PCS- Health Condition 2: K402- Bilateral inguinal hernia, withoutobstruction or gangreneHealth Condition 3: K929- Disease of digestive system, unspecifiedHealth Condition 4: K639- Disease of intestine, unspecifiedHealth Condition 5: K409- Unilateral inguinal hernia, without obstruction or gangrene

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: PCS- Health Condition 2: K402- Bilateral inguinal hernia, withoutobstruction or gangreneHealth Condition 3: K929- Disease of digestive system, unspecifiedHealth Condition 4: K639- Disease of intestine, unspecifiedHealth Condition 5: K409- Unilateral inguinal hernia, without obstruction or gangrene
Sponsor
All india institute of medical sciences Raipur
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Children of ASA 1 and 2 undergoing lower abdominal surgery

Exclusion Criteria

  • •Patients parents refusal
  • •Patients with any contraindications to regional anesthesia
  • •History of developmental delay or mental retardation, which will make observational pain intensity assessment difficult
  • •History of allergic reaction to local anesthetic
  • •Rash or skin infection at the site of injection
  • •Anatomical abnormalities
  • •Bleeding diathesis
  • •Coagulation disorder
  • •History of renal, hepatic, cardiac disorder, upper or lower airway infection or any neurological abnormalities.

Outcomes

Primary Outcomes

Not specified

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