Assessment of the incidence of surgical site infections after digestive surgery with preoperative oral antibiotics.

Assessment of the incidence of surgical site infections after digestive surgery with preoperative oral antibiotics. - Assessment of the incidence of surgical site infections after digestive surgery with preoperative oral antibiotics.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000015460

Enrollment

200

Registered

2014-12-01

Start date

2014-12-10

Completion date

Unknown

Last updated

2025-07-18

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

Conditions

Patients with lower digestive surgery (Inflammatory bowel disease, Colorectal cancer)

Interventions

oral antibiotics

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria:

Exclusion criteria

Exclusion criteria: Patients with allergy for Ciprofloxacin or Metronidazole.

Design outcomes

Primary

Measure	Time frame
The rate of surgical site infection at 30th days after surgery	—

Secondary

Measure	Time frame
Safety of the preoperative oral antibiotics.	—

Countries

Japan

Contacts

Public ContactKazuhiro Watanabe

Tohoku University Hospital Surgery

k-wata@surg1.med.tohoku.ac.jp+81-22-717-7205

Outcome results

None listed

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