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The efficacy of Sodium tetradecyl sulfate 1% and Ceftazidime and Metronidazole in perianal fistula

Comparison of the efficacy of Sodium tetradecyl sulfat 1% and Ceftazidime and Metronidazole in treatment of patients with perianal fistula

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013051913385N1
Enrollment
22
Registered
2013-08-07
Start date
2011-10-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Anal fistula. Anal fistula

Interventions

Intervention 1: Group 1: one day Sodium tetradecyl sulfate1% (1cc) diluted with 3cc water for injection and next day Ceftazidime (4cc) injected in fistula tract for 1 week, then 3 times in week until
Treatment - Drugs
Group 1: one day Sodium tetradecyl sulfate1% (1cc) diluted with 3cc water for injection and next day Ceftazidime (4cc) injected in fistula tract for 1 week, then 3 times in week until recovery occurr
Group 2: one day Sodium tetradecyl sulfate1% (1cc) diluted with 3cc water for injection and next day Metronidazole (4cc) injected in fistula tract for 1 week and then 3 times in week until recovery oc
Group 3: one day Ceftazidime (4cc) and next day Metronidazole (4cc) injected in fistula tract for 1 week and then 3 times in week until recovery occurred.

Sponsors

Ahvaz Jondishapur University of Medical Sciences, Vice Chancellor for Research and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patients with perianal fistula. Exclusion criteria: Pregnant or nursing women and patients with severe systemic disease.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Disappear of fistula tract. Timepoint: Six months after beginning of intervention. Method of measurement: Physical exam with prob.

Secondary

MeasureTime frame
Disappear of pain. Timepoint: Six months after beginning of intervention. Method of measurement: History.;Disappear of discharge. Timepoint: Six months after beginning of intervention. Method of measurement: History and Physical exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahtab Farhadi

Ahvaz Jondishapur University of Medical Sciences Surgery ward

bmohammadi13@yahoo.com+98 61 1222 7410

Outcome results

None listed

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