This randomized controlled trial aims to compare postoperative pain between staples and polypropylene sutures used for mesh fixation in patients undergoing elective Lichtenstein tension-free inguinal hernia repair.
Inguinal hernia repair is one of the most common general surgical procedures worldwide. The standard method for mesh fixation during Lichtenstein tension-free hernioplasty uses polypropylene sutures. However, skin staples have recently been introduced as a faster and potentially less painful alternative. This randomized controlled trial compares both methods in terms of postoperative pain, measured using the Visual Analogue Scale (VAS), and operative time.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
168
Mesh secured using stainless steel staples in Lichenstein tension-free inguinal hernioplasty
Mesh secured using polypropylene sutures in Lichenstein tension-free inguinal hernioplasty
Jinnah Postgraduate Medical Centre
Karachi, Sindh, Pakistan
RECRUITINGPostoperative pain (VAS score)
Pain intensity will be measured using the Visual Analogue Scale (VAS 0-10)
Time frame: Postoperative day 1, day 7 and day 30
Operative time (minutes)
Time in minutes from initiation of mesh fixation to completion of skin closure
Time frame: During Surgery (intraoperative period)
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