Viewing Study NCT06403774



Ignite Creation Date: 2024-05-11 @ 8:30 AM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06403774
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-05-08
First Post: 2024-04-20

Brief Title: Bowel Preparation Before Hemorrhoidectomy
Sponsor: Saglik Bilimleri Universitesi
Organization: Saglik Bilimleri Universitesi

Study Overview

Official Title: Effect of Two Different Bowel Preparation Methods on Outcomes After Hemorrhoidectomy
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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 heshe will be invited to participate in the study Written consent will be obtained from patients who agree to participate in the research

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None