Comparison of wound healing and complications of absorbable subcoticular suturing with steri-strips method with interrupted suturing method in uncomplicated appendicitis wound.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013040812948N1

Enrollment

Registered

2013-05-29

Start date

2012-10-22

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

Acute appendicitis. Acute appendicitis

Interventions

Intervention 1: Intervension group: absorbable subcoticular suturing with steri-strips in uncomplicated appendicitis. Intervention 2: Control group: interrupted suturing in wound of uncomplicated ap

Treatment - Surgery

Intervension group: absorbable subcoticular suturing with steri-strips in uncomplicated appendicitis.

Control group: interrupted suturing in wound of uncomplicated appendicitis.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients which candidate for appendectomy. and were entered in study after being informed about the study and receiving Informed consent. Exclusion criteria: perforated appendicitis, Gangrenous appendicitis, phlegmon of appendicitis, underlying disease such as diabetes?acquired or primary immunosuppression, difficulty in following patients

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Surgical site infection. Timepoint: at addmission, one week, one months, 3 months later. Method of measurement: physical examination.;Wound dehicence. Timepoint: at addmission, one week, one months, 3 months later. Method of measurement: physical examination.;Scar width. Timepoint: 3 months later. Method of measurement: millimeter.;Abcsess of wound site. Timepoint: at addmission, one week, one months, 3 months later. Method of measurement: physical examination.	—

Measure

Time frame

Surgical site infection. Timepoint: at addmission, one week, one months, 3 months later. Method of measurement: physical examination.;Wound dehicence. Timepoint: at addmission, one week, one months, 3 months later. Method of measurement: physical examination.;Scar width. Timepoint: 3 months later. Method of measurement: millimeter.;Abcsess of wound site. Timepoint: at addmission, one week, one months, 3 months later. Method of measurement: physical examination.

—

Secondary

Measure	Time frame
Patient satisfaction. Timepoint: at addmision, one month and 3 month later. Method of measurement: nominal scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Moein Lashkajani

Hamedan University of Medical Science

ali.moein@umsha.ac.ir+98 912 297 7591

Outcome results

None listed

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