To demonstrate that postoperative pain secondary to Milligan and Morgan hemorrhoidectomy with Caiman® (AESCULAP®) and subsequent oral conventional analgesia is at least not greater than that generated after hemorrhoidectomy with monopolar diathermy and intravenous analgesia with care home at discharge.
In the treatment of coloproctological pathology, one of the most important problems is postoperative pain. Especially in the management of hemorrhoids treatment. There are different approaches but in all of them pain is the predominant symptom. There are some less painful techniques but the gold standard continues to be hemmorrhoidectomy, which is associated with postoperative pain. Some actions have been taken to control pain to avoid the admission of patients, but there are still problems in this regard. Our group aims to study the effect of energy change for performing hemorrhoidectomy on postoperative pain.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
27
Hemorrhoidectomy with monopolar diathermy
Hemorrhoidectomy with Caiman® bipolar energy
Laura Mora López
Sabadell, Barcelona, Spain
RECRUITINGVisual analogue scale (VAS)
Postoperative pain: value 0 (no pain) - 10 (maximum pain)
Time frame: 6 hours of post-operative period (before hospital discharge performed); within 2 days with telephone control; at 7 days control at external consultations; at 30 days control at external consultations
Wound healing time
A healed wound is considered when all post-hemorrhoidectomy wounds of 2-3 bundles are epithelialized
Time frame: 7 days postoperative control at external consultations; 30 days postoperative control at external consultations
Post-surgery satisfaction survey
Phone checklist survey
Time frame: 30 days postoperative control at external consultations
Wexner scale
Assessment of fecal incontinence o a scale from 0 (never incontinence) to 4 (always), obtaining a score between 0 and 20.
Time frame: in pre-operative visit, on the 7th and 30th postoperative clinical control
Number of emergency consultations
revision of Database
Time frame: in 30 days post-surgery
Collection of adverse effects from patients
revision of Database
Time frame: in 30 days post-surgery
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