The Impact of Using Standard McBurney Incision and Davis Richey Incision in Surgery.
Conditions
Interventions
Intervention 1: The intervention group in this study consists of patients who will undergo appendectomy using the McBurney incision method. Intervention 2: The intervention group in this study consist
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The patient has appendicitis Providing informed and voluntary consent to participate in the study
Exclusion criteria
Exclusion criteria: Any history of psychiatric illness Phlegmonous appendicitis The withdrawal of a patient from the study at any stage of the study. Addiction Hematologic disorders Underlying diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patients pain level. Timepoint: After 6 hours of surgery. Method of measurement: VAS Scale.;Duration of surgery. Timepoint: Total time of surgery.("The time interval between the start of the surgical incision (the time of the first incision by the surgeon) and the completion of suturing.). Method of measurement: Minute.;Scar. Timepoint: Specialist follow-up after 3 months post-surgery. Method of measurement: Low/ Medium/ High. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSaman Kiani Afzali
Zahedan University of Medical Sciences
Outcome results
None listed