Comparison Between Single and Triple Rubber Band Ligation for the Treatment of Hemorrhoids
Primary Purpose
Second-degree Hemorrhoids
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Single hemorrhoidal ligation
Triple hemorrhoidal ligation
Sponsored by
About this trial
This is an interventional treatment trial for Second-degree Hemorrhoids focused on measuring Hemorrhoids, Ligation, Pain, Morbidity, Patient Satisfaction, Cost-Benefit Analysis
Eligibility Criteria
Inclusion Criteria:
- Patients with second-degree hemorrhoids
Exclusion Criteria:
- Patients with special needs
- Immunodepression
- Indians
- Infectious, inflammatory or tumoral anorectal comorbidities
- Previous anorectal surgeries
- Patients on anticoagulant therapy or with coagulation disorders
Sites / Locations
- Hospital Universitário Getúlio Vargas - Ambulatório Araújo Lima
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Single hemorrhoidal ligation
Triple hemorrhoidal ligation
Arm Description
Effective ligation of one hemorrhoidal group and sham ligation of the two other major hemorrhoidal groups is performed in each session of treatment.
The three major hemorrhoidal groups are ligated in the first session of ligation. The three following monthly appointments of patients of this arm are for sham hemorrhoidal ligations and final revision.
Outcomes
Primary Outcome Measures
Ligature-related pain intensity
Patients are asked to record pain intensity related to the hemorrhoidal ligation performed in a chart containing a modified pain intensity visual scale (Wong & Baker). Investigators inquire patients about immediate pain sensation after a ligation session and at regular intervals, by telephone calls, until the 7th post-treatment day (12 h, 24 h, 2nd day, 3rd day, 4th day, 5th day, 6th day and 7th day).
Secondary Outcome Measures
Immediate complications
Complications eventually ocurring until 30 days of each session of rubber band ligation of hemorrhoids (effective or sham) are recorded by the investigators.
Resolutive capacity of rubber band ligation of hemorrhoids
Resolution of pre-ligation hemorrhoidal symptoms is investigated 3 months after first session of rubber band ligation of hemorrhoids.
Degree of patient satisfaction
Three months after first session (or single session, according to the arm of treatment) of rubber band hemorrhoidal ligation each patient degree of satisfaction with the method is recorded analogously using the modified visual pain scale of Wong & Baker.
Costs of each of the modes of ligation
Three months after the first rubber band ligation session, the costs involved in each treatment modality is raised. Calculations are done taking into account the value of the material employed in all the ligation sessions that are necessary to treat each individual patient, the value of the fraction of the investigators' salaries compromised in the treatment of each individual patient, how much each patient spends in pain medication and the value of the fraction of the patients' salaries involved in occupational absenteeism.
Full Information
NCT ID
NCT01383577
First Posted
June 24, 2011
Last Updated
September 24, 2013
Sponsor
Federal University of Amazonas
1. Study Identification
Unique Protocol Identification Number
NCT01383577
Brief Title
Comparison Between Single and Triple Rubber Band Ligation for the Treatment of Hemorrhoids
Official Title
Double-blind Randomized Controlled Study of Single Versus Triple Rubber Band Ligation of Hemorrhoids
Study Type
Interventional
2. Study Status
Record Verification Date
September 2013
Overall Recruitment Status
Unknown status
Study Start Date
March 2010 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
November 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of Amazonas
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Rubber band ligation is a widely adopted treatment of internal hemorrhoids in busy coloproctology institutions. All three major hemorrhoidal clusters (left lateral, right anterior and right posterior) use to be ligated in order to obtain therapeutic success. It is commonly performed either through the ligation of a single hemorrhoid per session spaced by some few weeks to the second and third sessions, or of all three major hemorrhoids in one single session. Advocates of either method of hemorrhoidal ligation have arguments to defend their choice in terms of advantages, supported mainly on personal preferences. The investigators objective is to determine, through a controlled double-blinded randomized study, if there is any superiority of single hemorrhoidal ligation per session (in a total of three sessions) over the method of ligation of all three main hemorrhoids in a sole session in terms of therapeutic success (resolution of pre-ligation symptoms), morbidity, patient satisfaction and costs (institutional, labor and patient-related).
Detailed Description
Because of conflicting results in existing literature in relation to features such as pain and immediate effectiveness of single or multiple rubber band ligation of hemorrhoids and because in the literature consulted no study was found that addressed economical features comparing single with multiple rubber band ligation of hemorrhoids, this study was designed to compare, in a double blinded, randomized and controlled model, the results of single hemorrhoidal ligation in three sessions with triple hemorrhoidal in a sole session in terms of immediate effectiveness, patient satisfaction and costs.
Patients enrolled in the study, after applying inclusion and exclusion criteria, signed the consent form, and responded to a questionaire about epidemiological data and hemorrhoidal symptoms, are (and will be) randomly allocated to one of the two arms of the study: G1: a single major hemorrhoidal group is ligated in each of three sessions of hemorrhoidal ligation, while the two other hemorrhoidal groups are submitted to sham ligation (a McGown aspirating type of hemorrhoidal ligator is employed); G2: all three major hemorrhoidal groups are ligated in the first session of treatment and in the next two sessions only sham ligations are performed. Three sessions of hemorrhoidal and/or sham ligation are performed in all patients, each spaced by one month from the other. A final consultation is held 1 month after the third ligation session in order to gather all the results of the treatment.
After each session of hemorrhoidal ligation patients receive a chart containing a modified level of pain scale (Wong & Baker) and are asked to indicate pain level (from 0 to 5: 0 = no pain, 5 = unbearable pain) at fixed intervals (immediate post-ligation, 12 h post-ligation, 24 h post-ligation and each other day until 7 days post-ligation). Investigators gather this information about pain, and patient well-being post-ligations, from 8 programmed telephone calls to the patients after each session of hemorrhoidal (or sham) ligation.
Three months after the first session of hemorrhoidal ligation all patients are examined in order to observe treatment effectiveness and gather data about complications, patient satisfaction, number of days of occupational absenteeism linked to each session of treatment and number of analgesic pills necessary for pain relief.
Comparative costs of each modality of ligation are raised taking into consideration the salaries of health professionals involved in the treatment, the salaries of the patients (calculation of absenteeism), the value of consumables used in each session of effective ligation, the depreciation price of permanent material employed and the price of medications patients have to buy.
Patients are blinded to the modality of hemorrhoidal ligation employed and the statistician does not know the nature of each treatment group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Second-degree Hemorrhoids
Keywords
Hemorrhoids, Ligation, Pain, Morbidity, Patient Satisfaction, Cost-Benefit Analysis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
76 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Single hemorrhoidal ligation
Arm Type
Experimental
Arm Description
Effective ligation of one hemorrhoidal group and sham ligation of the two other major hemorrhoidal groups is performed in each session of treatment.
Arm Title
Triple hemorrhoidal ligation
Arm Type
Experimental
Arm Description
The three major hemorrhoidal groups are ligated in the first session of ligation. The three following monthly appointments of patients of this arm are for sham hemorrhoidal ligations and final revision.
Intervention Type
Procedure
Intervention Name(s)
Single hemorrhoidal ligation
Other Intervention Name(s)
Rubber band ligation of hemorrhoids, single
Intervention Description
Effective ligation of one hemorrhoidal group and sham ligation of the two other major hemorrhoidal groups is performed in each of three sessions of treatment. Final revision is performed 90 days after first session of hemorrhoidal ligation.
Intervention Type
Procedure
Intervention Name(s)
Triple hemorrhoidal ligation
Other Intervention Name(s)
Rubber band ligation of hemorrhoids, multiple
Intervention Description
The three major hemorrhoidal groups are ligated in the first session of ligation. Sham triple hemorrhoidal ligations are performed 30 and 60 days after the first session. Final revision is done 90 days after first ligation session.
Primary Outcome Measure Information:
Title
Ligature-related pain intensity
Description
Patients are asked to record pain intensity related to the hemorrhoidal ligation performed in a chart containing a modified pain intensity visual scale (Wong & Baker). Investigators inquire patients about immediate pain sensation after a ligation session and at regular intervals, by telephone calls, until the 7th post-treatment day (12 h, 24 h, 2nd day, 3rd day, 4th day, 5th day, 6th day and 7th day).
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Immediate complications
Description
Complications eventually ocurring until 30 days of each session of rubber band ligation of hemorrhoids (effective or sham) are recorded by the investigators.
Time Frame
30 days
Title
Resolutive capacity of rubber band ligation of hemorrhoids
Description
Resolution of pre-ligation hemorrhoidal symptoms is investigated 3 months after first session of rubber band ligation of hemorrhoids.
Time Frame
90 days
Title
Degree of patient satisfaction
Description
Three months after first session (or single session, according to the arm of treatment) of rubber band hemorrhoidal ligation each patient degree of satisfaction with the method is recorded analogously using the modified visual pain scale of Wong & Baker.
Time Frame
90 days
Title
Costs of each of the modes of ligation
Description
Three months after the first rubber band ligation session, the costs involved in each treatment modality is raised. Calculations are done taking into account the value of the material employed in all the ligation sessions that are necessary to treat each individual patient, the value of the fraction of the investigators' salaries compromised in the treatment of each individual patient, how much each patient spends in pain medication and the value of the fraction of the patients' salaries involved in occupational absenteeism.
Time Frame
90 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with second-degree hemorrhoids
Exclusion Criteria:
Patients with special needs
Immunodepression
Indians
Infectious, inflammatory or tumoral anorectal comorbidities
Previous anorectal surgeries
Patients on anticoagulant therapy or with coagulation disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ivan T Costa e Silva, PhD
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Érico L Melo, Med Grad
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Giselle L Afonso, Med Grad
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Felicidad S Gimenez, MSc
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Shymmene O Cardoso, BAccount
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Daniel Richard M Mota, Med Grad
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rachel M Carvalho, Med Grad
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Saskia Regina F Coppens, Med Grad
Organizational Affiliation
Universidade Federal do Amazonas
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Themis C Abensur, MSc
Organizational Affiliation
Federal University of Amazonas
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital Universitário Getúlio Vargas - Ambulatório Araújo Lima
City
Manaus
State/Province
Amazonas
ZIP/Postal Code
69020-160
Country
Brazil
12. IPD Sharing Statement
Learn more about this trial
Comparison Between Single and Triple Rubber Band Ligation for the Treatment of Hemorrhoids
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