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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05605080
Other study ID # N202209015
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 7, 2022
Est. completion date November 20, 2023

Study information

Verified date November 2023
Source Taipei Medical University Shuang Ho Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the hemostatic and analgesic effect of using gauze with Bosmin or Gelfoam after anal surgery.


Description:

Hemorrhoidectomy and fistulotomy these two types of anal surgery are common surgeries in colon and rectal surgery division in Shuang Ho hospital. For these patients underwent surgical treatment, some surgeons used gauze with Bosmin for hemostasis and analgesia after surgery, and other surgeons used Gelfoam. These choices were often determined by surgeon's personal preference according to their experiences. Shuang Ho hospital has top three quantity of hemorrhoidectomy in Taiwan. So, a randomized controlled trial is conducted to evaluate the difference between hemostatic agents use after anal surgery.


Recruitment information / eligibility

Status Completed
Enrollment 292
Est. completion date November 20, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 85 Years
Eligibility Inclusion Criteria: - Patients who undergo conventional hemorrhoidectomy or stapled hemorrhonidpexy are include. - Patients who undergo fistulectomy or fistulotomy are include. Exclusion Criteria: - Emergency operation - Patients with colorectal cancer - Liver cirrhosis - Patients with coagulopathy - Patients with HIV infection

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Gelfoam
Use Gelfoam as a hemostatic agent after anal surgery.
Other:
Bosmin gauze
Use bosmin gauze as a hemostatic agent after anal surgery.

Locations

Country Name City State
Taiwan Taipei Medical University Shuang-Ho Hospital New Taipei City

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University Shuang Ho Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Post-operative pain Record maximum pain score (visual analog scale, 0-10) from post-operative day 0 to day 7. 0-7 days
Primary Analgesic agent use Daily consumption of oral analgesics from post-operative day 0 to day 7 0-7days
Secondary Incidence of post-operative bleeding Postoperative delayed bleeding was defined as (1) when the bleeding required surgical intervention or (2) when hospital re-admission was warranted after patient discharge. 0-30 days
Secondary Incidence of urinary retention Urinary retention was defined as patients requiring Foley catheterization during the hospital stay 0-7 days
Secondary Incidence of surgical site infection Surgical site infection was defined as hospital admission for infection management or need for surgical intervention to manage the wound. 0-30 days
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