The comparison of single incision laparoscopic appendectomy and conventional laparoscopic appendectomy

The comparison of short time outcomes between single incision laparoscopic appendectomy and conventional laparoscopic appendectomy surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220530055027N1

Enrollment

Registered

2022-10-15

Start date

2022-12-23

Completion date

Unknown

Last updated

2022-11-21

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

Conditions

Condition 1: Single incision laparoscopic appendectomy (SILA). Condition 2: Conventional laparoscopic appendectomy. Acute appendicitis Acute appendicitis

Interventions

Intervention 1: Intervention group: Single-incision laparoscopic appendectomy. Intervention 2: Control group: Conventional laparoscopic appendectomy.

Eligibility

Sex/Gender

All

Age

1 Years to 20 Years

Inclusion criteria

Inclusion criteria: Consent to participate in the research Age under 20 years Stable patient

Exclusion criteria

Exclusion criteria: Over 20 years old Abdominal infection Emergency Case Pregnancy Perforated appendicitis

Design outcomes

Primary

Measure	Time frame
The degree of beauty of the operation site. Timepoint: Up to 3 weeks after surgery. Method of measurement: Based on the PSQ questionnaire.;The amount of pain after the operation. Timepoint: Up to 3 weeks after surgery. Method of measurement: Based on the VAS questionnaire.;Types of complications after surgery. Timepoint: Up to 3 weeks after surgery. Method of measurement: Self-Report.;Duration of operation. Timepoint: During surgery. Method of measurement: Based on the duration of surgery.;Duration of hospitalization. Timepoint: From after surgery to discharge. Method of measurement: Record the number of days of hospitalization.;Duration of leukocytosis drop. Timepoint: It is measured once before the operation and once or twice after the operation. Method of measurement: Record the duration of leukocytosis drop.	—

Measure

Time frame

The degree of beauty of the operation site. Timepoint: Up to 3 weeks after surgery. Method of measurement: Based on the PSQ questionnaire.;The amount of pain after the operation. Timepoint: Up to 3 weeks after surgery. Method of measurement: Based on the VAS questionnaire.;Types of complications after surgery. Timepoint: Up to 3 weeks after surgery. Method of measurement: Self-Report.;Duration of operation. Timepoint: During surgery. Method of measurement: Based on the duration of surgery.;Duration of hospitalization. Timepoint: From after surgery to discharge. Method of measurement: Record the number of days of hospitalization.;Duration of leukocytosis drop. Timepoint: It is measured once before the operation and once or twice after the operation. Method of measurement: Record the duration of leukocytosis drop.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarges Khaleghi Rostamkolaie

Karaj University of Medical Sciences

atousakhaleghi71@gmail.com+98 21 4410 8369

Outcome results

None listed

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