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A comparison between the two different anesthetic technique(caudal block and dorsal penile block) for post operative pain relief in circumcision surgery among the pediatric populations

Comparison of relative efficacy between caudal block and dorsal penile nerve block in circumcision surgery among paediatric populations( upto 12 years of age) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064469
Enrollment
110
Registered
2024-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N475- Adhesions of prepuce and glans penis

Interventions

Intervention1: CAUDAL BLOCK for GROUP C populations. : In GROUP C (CAUDAL BLOCK), all the allotted patients will be given caudal block (after initiation of general anaesthesia as mentioned above) at

Sponsors

Department of anesthesiology KPC Medical College Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Only ASA(AMERICAN SOCIETY OF ANAESTHESIA)1 category ( no comorbidities) male children will be selected. 2.Male children below 12 years of age will selected. 3.Only planned circumcision surgeries will considered.

Exclusion criteria

Exclusion criteria: 1.Participants/parents who are not willing to undergo any survey even after proper explanation. 2.Male children beyond category ASA(AMERICAN SOCIETY OF ANAESTHESIA)1. 3.Any emergency genitourinary surgeries where circumcision will be requiring. 4.Local site infection where infiltration of regional anesthesia will be given. 5.Presence of any coagulopathy. 6.Patient who are allergic to anesthetic agents. 7.Anatomical anomalies like spinal anomalies, pilonidal cyst etc at caudal space.

Design outcomes

Primary

MeasureTime frame
To compare the relative efficacy of post operative analgesia between caudal block and dorsal penile nerve block in circumcision surgery among paediatric populations( upto 12 years)Timepoint: After application of two different techniques 1st ,6th,12th and 24th hour the efficacy of analgesia of two different techniques will be assessed by CHEOPS scale for pain and sedation score with RSS along with measuring noninvasive blood pressure and pulse—

Secondary

MeasureTime frame
Along with primary outcome any untoward secondary outcomes or complications related to the procedure ( if any)during the entire study will also be assessed Timepoint: Assessment of untoward effects will be done during the assessment of pain & sedation along the vitals at 1st,6th, 12th & 24th hour of application of the procedures.—

Countries

India

Contacts

Public ContactDr Sukanta Majumder

KPC MEDICAL COLLEGE AND HOSPITAL

sarkarchiranjib@yahoo.in9163692003

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026