Pain and Bleeding in Subjects With Acute Anal Fissure: Comparative Evaluation of Three Treatments (PBSAAF)
Primary Purpose
Acute Anal Fissure
Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Centella
Proctocella
Flavonil® cps
Flavonil® Cream
Rectalgan Mousse
Sponsored by
About this trial
This is an interventional treatment trial for Acute Anal Fissure focused on measuring Anal Fissure, local therapy, pain, defecation, bleeding
Eligibility Criteria
Inclusion Criteria:
- Subjects With Acute Anal Fissure
- Collaborative patients able to understand and want;
Exclusion Criteria:
- Pregnancy
Sites / Locations
- Department of General Surgery "Paride Stefanini", University of Rome "La Sapienza"
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm Type
Experimental
Experimental
Experimental
Experimental
Experimental
Arm Label
AAF treated with Centella® Complex
AAF treated with Proctocella® cream
AAF treated with Flavonil® cps
AAF treated with Flavonil® Cream
AAF treated with Rectalgan Mousse
Arm Description
Centella® Complex 1 cps 60 mg per os
Proctocella® Complex cream to be applied in anal area and anal canal
Flavonil® 1 cps 300 mg per os
Flavonil® Cream Cream to be applied in anal region and anal canal
Rectalgan Mousse cleansing cleanser for anal and perineal region
Outcomes
Primary Outcome Measures
time for the disappearance of pain
time for the disappearance of pain in course of treatment
Secondary Outcome Measures
time for the disappearance of bleeding
time for the disappearance of bleeding in course of treatment
Full Information
NCT ID
NCT03355846
First Posted
November 22, 2017
Last Updated
July 11, 2018
Sponsor
University of Roma La Sapienza
1. Study Identification
Unique Protocol Identification Number
NCT03355846
Brief Title
Pain and Bleeding in Subjects With Acute Anal Fissure: Comparative Evaluation of Three Treatments
Acronym
PBSAAF
Official Title
Pain and Bleeding in Subjects With Acute Anal Fissure: Comparative Evaluation of Three Treatments
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
May 1, 2018 (Actual)
Primary Completion Date
May 1, 2018 (Actual)
Study Completion Date
May 1, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Roma La Sapienza
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Starting from the observation that acute anal fissure (AAF) in 6-8 weeks can heal spontaneously and that some of the commonly used commercial products in clinical practice would seem to be useful, the rationale of the comparative study is to try to identify, in compliance with the protocol of Helsinki (2013), the most effective short-term treatment for the disappearance of pain in defecation and cessation of bleeding, shortening the duration of the healing process and favoring the patient's rapid return to his / her activity, respect for patient safety.
Detailed Description
Starting from the observation that anal fissure in 6-8 weeks can heal spontaneously and that some of the commonly used commercial products in clinical practice would seem to be useful, the rationale of the comparative study is to try to identify, in compliance with the protocol of Helsinki (2013), the most effective short-term treatment for the disappearance of pain in defecation and cessation of bleeding, shortening the duration of the healing process and favoring the patient's rapid return to his / her activity, respect for patient safety.
The comparative study will be conducted by comparing the following products:
Centella® Complex 1 cps 60 mg per os after meals twice a day for 15 days;
Proctocella® Complex cream to be applied in anal area and anal canal after hygiene treatment for 4 weeks;
Flavonil® 1 cps 300 mg per os after meals twice a day for 15 days;
Flavonil® Cream Cream to be applied in anal region and anal canal after hygiene treatment for 4 weeks;
Rectalgan Mousse cleansing cleanser for anal and perineal region for 4 weeks.
Our approach attempts to blend, based on the evidence of the most recent scientific literature, the experience of decades of colonproctologic clinical practice that has a predominantly surgical approach, with the clinical evidence of the Science of Nutrition which has a conservative vision in the treatment of ailments and constipation, a predisposing factor in the pathogenesis of anal fissure, in order to obtain healing without surgery. The control group will receive the traditional basic treatment consisting in the application of lubricated anal dilators of increasing gauge according to predetermined pattern, hygiene and diet. The two groups with which they will be compared for the results will receive, in addition to the foregoing (for controls), or Flavonoids (ProtFlav) or Asian Centella Extract (ProtCent), in the form of local mouth and cream tablets to be applied at the perianal level and possibly in the anal canal with gloved finger, containing the same active principles also administered by mouth.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Anal Fissure
Keywords
Anal Fissure, local therapy, pain, defecation, bleeding
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
99 (Actual)
8. Arms, Groups, and Interventions
Arm Title
AAF treated with Centella® Complex
Arm Type
Experimental
Arm Description
Centella® Complex 1 cps 60 mg per os
Arm Title
AAF treated with Proctocella® cream
Arm Type
Experimental
Arm Description
Proctocella® Complex cream to be applied in anal area and anal canal
Arm Title
AAF treated with Flavonil® cps
Arm Type
Experimental
Arm Description
Flavonil® 1 cps 300 mg per os
Arm Title
AAF treated with Flavonil® Cream
Arm Type
Experimental
Arm Description
Flavonil® Cream Cream to be applied in anal region and anal canal
Arm Title
AAF treated with Rectalgan Mousse
Arm Type
Experimental
Arm Description
Rectalgan Mousse cleansing cleanser for anal and perineal region
Intervention Type
Drug
Intervention Name(s)
Centella
Intervention Description
after meals twice a day for 15 days
Intervention Type
Drug
Intervention Name(s)
Proctocella
Intervention Description
after hygiene treatment for 4 weeks;
Intervention Type
Drug
Intervention Name(s)
Flavonil® cps
Intervention Description
after meals twice a day for 15 days
Intervention Type
Drug
Intervention Name(s)
Flavonil® Cream
Intervention Description
treatment for 4 weeks;
.
Intervention Type
Drug
Intervention Name(s)
Rectalgan Mousse
Intervention Description
for 4 weeks
Primary Outcome Measure Information:
Title
time for the disappearance of pain
Description
time for the disappearance of pain in course of treatment
Time Frame
1 month
Secondary Outcome Measure Information:
Title
time for the disappearance of bleeding
Description
time for the disappearance of bleeding in course of treatment
Time Frame
1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects With Acute Anal Fissure
Collaborative patients able to understand and want;
Exclusion Criteria:
Pregnancy
Facility Information:
Facility Name
Department of General Surgery "Paride Stefanini", University of Rome "La Sapienza"
City
Rome
State/Province
RM
ZIP/Postal Code
00161
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
12135106
Citation
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Results Reference
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Results Reference
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PubMed Identifier
12188628
Citation
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Results Reference
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
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Citation
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Results Reference
result
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Pain and Bleeding in Subjects With Acute Anal Fissure: Comparative Evaluation of Three Treatments
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