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Clinical Trials/NCT06403774
NCT06403774
Enrolling By Invitation
Not Applicable

Effect of Two Different Bowel Preparation Methods on Outcomes After Hemorrhoidectomy

Saglik Bilimleri Universitesi1 site in 1 country60 target enrollmentJuly 1, 2023

Overview

Phase
Not Applicable
Intervention
Group that will undergo bowel preparation using laxatives (Two bowel X-M Solution 250 ml.)
Conditions
HEMORRHOIDECTOMY
Sponsor
Saglik Bilimleri Universitesi
Enrollment
60
Locations
1
Primary Endpoint
Pain level
Status
Enrolling By Invitation
Last Updated
last year

Overview

Brief Summary

The purpose of this research; To evaluate the effect of preoperative bowel preparation on post-hemorrhoidectomy outcomes. Bowel preparation is a routine practice before surgery in anorectal diseases. This study aims to evaluate the effect of bowel preparation using laxatives or enemas on the patient postoperative pain, analgesic consumption amount, comfort, first defecation time and satisfaction, and to evaluate the satisfaction of the surgical team.

Detailed Description

The study is planned as a semi-experimental. The effect of bowel preparation using laxatives or enemas on postoperative pain, analgesic consumption, comfort and satisfaction will be evaluated. Criteria for inclusion in the research; Being a patient who will undergo hemorrhoidectomy with spinal anesthesia and agreeing to participate in the study are the exclusion criteria; Refusal to participate in the research was determined as. Following the admission of the patient, who is planned to undergo hemorrhoidectomy, to the clinic, the patient will be interviewed, the purpose of the study will be explained and he/she will be invited to participate in the study. Written consent will be obtained from patients who agree to participate in the research.

Registry
clinicaltrials.gov
Start Date
July 1, 2023
End Date
May 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bediye Öztaş

Principal investigator

Saglik Bilimleri Universitesi

Eligibility Criteria

Inclusion Criteria

  • Being a patient who will undergo hemorrhoidectomy surgery with spinal anesthesia
  • Agreeing to participate in the study

Exclusion Criteria

  • Not accepting participation in the study

Arms & Interventions

Group that will undergo bowel preparation using laxatives (Two bowel X-M Solution 250 ml.)

Bowel preparation will be made using a laxative (Two bowel X-M Solution 250 ml.)

Intervention: Group that will undergo bowel preparation using laxatives (Two bowel X-M Solution 250 ml.)

Group that will undergo bowel preparation using enema (Two bowel E.S. Enema )

Bowel preparation will be made using enema (Two bowel E.S. Enema )

Intervention: Group that will undergo bowel preparation using enema (Two bowel E.S. Enema )

Outcomes

Primary Outcomes

Pain level

Time Frame: postoperative 2, 6, 10, 20, 24. hours and at the first defecation assessed up to 72 hours

To evaluate pain; A numerical rating scale will be used, numbered 0-10, 0: no pain, 10: unbearable pain (1-3 mild, 4-6 moderate, 7-10 severe).

Secondary Outcomes

  • Comfort level(It will be evaluated once at the 24th postoperative hour.)
  • Satisfaction level of patients(It will be evaluated once at the 24th postoperative hour.)
  • Analgesic consumption amount(First 24 hours postoperatively)

Study Sites (1)

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