Effect of Enhanced Recovery After Surgery for Benign Anorectal Conditions

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMansoura University

About this trial

This study aims to assess the role of Enhanced recovery after surgery(ERAS) protocol in reducing postoperative urine retention (POUR) after surgery for benign anorectal conditions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

both sexes

aged between 18 and 65 years old

presented with benign anorectal conditions including chronic anal fissure, hemorrhoids, and fistula-in-ano will be eligible for the study

Disqualifiers

younger than 18

older than 65 years old

pregnant female

history of relevant urological diagnosis (benign prostatic hyperplasia/prostate cancer/urethral stricture/bladder neck stenosis/detrusor underactivity/detrusor overactivity)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Enhanced recovery after surgery protocol

    Other intervention

    ERAS pathway was developed based on the available guidelines and protocols it includes 14 items: 1. Preoperative patient education using an information sheet which includes instructions on postoperative wound care, pain management, and preventing and managing constipation. 2. Single preoperative enema 2 hours prior to surgery. 3. Solid or semisolid food stopped 6 hours before surgery. 4. Clear liquids may be continued up to 2 hours before surgery. 5. Preoperative carbohydrate loading in non-diabetic patients for up to 2 hours prior to surgery in the form of a single 330 ml high-carbohydrate clear drink (apple juice). 6. Saddle anesthesia. 7. Single dose of intravenous 500 mg metronidazole at the time of the anaesthesi induction. 8. Restriction of intraoperative intravenous fluids to less than 500 ml. 9. Balanced chloride-restricted crystalloid solutions should be used for maintenance infusions and fluid boluses. 10. A bundle measures to reduce surgical site infection which includes

  • Routine pathway

    Other intervention

    This is the routine preoperative preparation at our institute

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Enhanced recovery after surgery protocolActive comparator 1 intervention
Group B: Routine practiceOther 1 intervention

Trial outcomes

Primary outcomes

1

72-hours postoperative urinary retention after anorectal surgery

the inability to void, with the patient needing bladder decompression by catheterization as determined by the treating clinician within 1 week of surgery

Time frame
72 hours after surgery

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.