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A study in boys undergoing circumcision to compare two types of electric surgical tools and their effects on operation time, bleeding, infection, and healing

Comparative Evaluation of Monopolar versus Bipolar Electrocautery in Pediatric Circumcision: A Randomized Controlled Trial Assessing Outcomes. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108291
Enrollment
80
Registered
2026-04-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Monopolar electrocautery-assisted circumcision : Participants randomized to this arm will undergo circumcision using monopolar electrocautery in pure-cut mode at low wattage and brief
duration corresponds to operative time, typically 15 30 minutes per participant. Control Intervention1: Bipolar electrocautery-assisted circumcision : Participants randomized to this arm will underg
duration corresponds to operative time, typically 15 30 minutes per participant.

Sponsors

Multi Disciplinary Research Unit MDRU Netaji Subhash Chandra Bose Medical College Jabalpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Boys aged 6 months to 10 years ASA I II Elective circumcision Parental consent for participation and photography

Exclusion criteria

Exclusion criteria: Bleeding disorder, Infants <6 months, penile anomalies, infection, adrenaline use, prior penile surgery.

Design outcomes

Primary

MeasureTime frame
Operative time (minutes) Timepoint: The primary outcome will be operative time (in minutes), defined as the duration from the first incision to completion of the last skin suture, and it will be assessed during the surgical procedure for each enrolled participant.

Secondary

MeasureTime frame
Intraoperative/postoperative bleeding requiring intervention Surgical site infection Postoperative edema (graded via blinded assessment) Time to complete epithelialization (healing) Energy-related complications (ischemia, necrosis) Need for reoperation Timepoint: Intraoperative/postoperative bleeding requiring intervention Surgical site infection within 14 days of surgery Postoperative edema (graded via blinded assessment) within 14 days of surgery Time to complete epithelialization (healing) 15 days to 6 weeks Energy-related complications (ischemia, necrosis) within 14 days Need for reoperation within 3 months

Countries

India

Contacts

Public ContactDr Himanshu Acharya

NSCB Medical college Jabalpur MP

dr.himanshu.acharya.mch@gmail.com9926277512

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026