Evaluation of preoperative pediatric umbilical preparation using olanexidine gluconate

Evaluation of preoperative pediatric umbilical preparation using olanexidine gluconate - Evaluation of preoperative pediatric umbilical preparation using olanexidine gluconate

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000037649

Enrollment

Registered

2019-08-13

Start date

2019-08-09

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Pediatric patients receiving laparoscopic surgery

Interventions

Control 20cases Chlorhexidine Gluconate 20cases Oranedine Gluconate 20cases

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Pediatric patients receiving operation of inguinal hernia, retension testis or benign tumor resction

Exclusion criteria

Exclusion criteria: 1 serious conditon 2 emergency operation 3 exposing mucosal membrane in the umblicum 4 dermatitis in the umblicum 5 drug allergy 6 other inadequate conditon

Design outcomes

Primary

Measure	Time frame
Population and numberof bacteria after umbilical disinfection	—

Countries

Japan

Contacts

Public ContactObatake Masayuki

Kochi Medical School Hospital Surgery 1

mobatake@kochi-u.ac.jp088-880-2370

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026